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Tytuł:
Differential diagnosis between fibromyalgia syndrome and myofascial pain syndrome
Autorzy:
Chochowska, M.
Szostak, L.
Marcinkowski, J.T.
Jutrzenka-Jesion, J.
Powiązania:
https://bibliotekanauki.pl/articles/3306.pdf
Data publikacji:
2015
Wydawca:
Instytut Medycyny Wsi
Tematy:
diagnosis
fibromyalgia syndrome
myofascial pain syndrome
trigger mechanism
human disease
Opis:
Introduction. Fibromyalgia syndrome (FMS) and myofascial pain syndrome (MFPS) can be ranked among disease entities being difficult to diagnose clinically, manifesting themselves mainly through pain in specific hypersensitivity points. Aim. To present the current state of medical knowledge about pain spots appearing on hypersensitive points of soft tissue in the context of selected disease entities. Summary of the knowledge. MFPS is defined as sensory, motor and autonomic complaints, caused by the occurrence of trigger points (TrP). Yet the FMS is stated during the anamnesis on the basis of generalized pain, and pressure achiness of at least 11 out of 18 tender points (TP) of precisely determined location. Patients with FMS report numerous additional complaints – apart from the above mentioned ones; these are however highly non-specific and are not confirmed during routine medical check-ups. There are also no laboratory tests that can confirm presence of TrP being characteristic to MFPS and differentiating it from other muscles’ disease entities. Such points are identified only with the use of palpation. Unfortunately while examining a patient this way TrP – being symptoms of MFPS – can be quite easily confused with TP – being symptoms of FMS. Patients with MFPS which is developing in consequence of long-lasting global disorder of muscle tension balance and sensitivity of nociceptors as a result of chronically remaining pain, frequently suffer from achiness fulfilling the criteria of generalized pain. Moreover – in effect of static overload of soft tissues (especially of tonic muscles) – there occur hypersensitive palpable areas (points). Stimulating them cause lively reaction of the patient. Described symptoms can suggest a suspicion of FMS – the more so that making a diagnosis of MFPS does not exclude its coexistence. Having this in mind, there is a pretty large group of authors who raise a supposition that the differential diagnosis between TrP and TP should be observed in the quantitative rather than in the qualitative categories, despite the still binding definition and nomenclature. Recapitulation. Looking at the MFPS and at the FMS from the perspective of evolution of knowledge about them and from the point of view of period when scientific researches were conducted and their results published, it must be stated that during last years a considerable progress has been obtained in scope of better understanding of pathogenesis and pathophysiology of pain in specified points of soft tissue hypersensitivity, and the parallel clinical studies – confirming the hypotheses that were made – clearly increased the diagnostic and therapeutic capabilities of clinical practice.
Źródło:
Journal of Pre-Clinical and Clinical Research; 2015, 09, 1
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
New approach to Caplan’s syndrome
Autorzy:
Brzeski, Z.
Sodolski, W.
Powiązania:
https://bibliotekanauki.pl/articles/3314.pdf
Data publikacji:
2008
Wydawca:
Instytut Medycyny Wsi
Tematy:
human disease
Caplan’s syndrome
Caplan disease zob.Caplan's syndrome
rheumatoid pneumoconiosis zob.Caplan’s syndrome
collagen pneumoconiosis
rheumatoid arthritis
Źródło:
Journal of Pre-Clinical and Clinical Research; 2008, 02, 2
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Delusional Misidentification Syndrome: dissociation between recognition and identification processes
Autorzy:
Leis, Kamil
Mazur, Ewelina
Racinowski, Mariusz
Jamrożek, Tomasz
Gołębiewski, Jakub
Gałązka, Przemysław
Pąchalska, Maria
Powiązania:
https://bibliotekanauki.pl/articles/2106025.pdf
Data publikacji:
2019-12-18
Wydawca:
Fundacja Edukacji Medycznej, Promocji Zdrowia, Sztuki i Kultury Ars Medica
Tematy:
intermetamorphosis syndrome
Fregoli syndrome
Capgras syndrome
delusional misidentification syndromes
schizophrenia
Opis:
Delusional misidentification syndrome (DMS) is an umbrella term for syndromes of intermetamorphosis, Fregoli, and Capgras. DMS) is thought to be related to dissociation between recognition and identification processes. DMS was described for the first time in 1932 as a variant of the Capgras syndrome and is currently on the DSM-V list of diseases as an independent disease entity. Patients affected by DMS believed that people around them, most often family, have changed physically (appearance) and mentally (character). Other symptoms include confabulation, derealization or depersonalization. In patients, aggressive behavior is often observed, aimed at alleged doppelgangers resulting from the sense of being cheated and manipulated. With the intermetamorphosis syndrome, for example, schizophrenia, depression, bipolar disorder or other misidentification syndromes (Fregoli's, Capgras) may coexist. There is also a reverse intermetamorphosis, where the object of the changed appearance or character becomes the patient himself. One of its forms may be lycanthropy. The etiology of the intermetamorphosis has not been fully understood, one of the reasons may be brain damage and changes in the parietal and/or temporal lobes of the right hemisphere. It may then damage long neuronal connections to the frontal areas of the brain, disturbances of working memory (WM) accountable for the keep and online management of data, so that it is available for further processing, and the patient's will be uncritical. The basic method of diagnosis of this delusion is a medical interview with the patient. Other diagnostic methods include computed tomography, magnetic resonance imaging, EEG and ERPs. Experimental methods include searching for the neuromarker of DMS. Currently, there are no treatment guidelines of this delusional disorder, and pharmacotherapy experimental, but the drugs from the group of neuroleptics and lithium seem effective. Some hope for the treatment is created by neurotherapy, but it is also experimental.
Źródło:
Acta Neuropsychologica; 2019, 17(4); 456-467
1730-7503
2084-4298
Pojawia się w:
Acta Neuropsychologica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Assessment of surgical treatment of Eagle’s syndrome
Autorzy:
Czajka, Marcin
Szuta, Mariusz
Zapała, Jan
Janecka, Iga
Powiązania:
https://bibliotekanauki.pl/articles/1397804.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
Eagle’s syndrome
odynophagia
stylocarotid syndrome
styloid process
Opis:
Introduction: The aim of the study was to assess the effectiveness of surgical treatment of patients with Eagle’s syndrome, taking into account both early and late results. Material and methods: The study group consisted of 15 patients who underwent resection of the styloid process due to Eagle syndrome in the period of 2005–2017. During the follow-up visit, the patients were asked to fill in a post-operative questionnaire that compared the pre-operative symptoms and their severity with the patients’ current health condition. The VAS pain scale was used to assess each symptom, and the Laitinen scale was used to assess the quality of life. Data from patients’ medical records were also included. The results of the surveys were subjected to statistical analysis. Results: The study showed that in 11 out of 15 cases there was a significant improvement in the level of pain (70.5% on average) and an improvement in quality of life (on average 65%) comparing to the pre-operative condition. The Wilcoxon test for binding pairs, the Mann-Whitney test, the Kruskal-Wallis test and the Spearman correlation coefficient were used in the statistical analysis. There were statistically significant correlations between the recorded improvement rate and the length of the resected styloid process and its setting. Discussion: The study proved that resection of prolonged styloid process from extraoral approach in most cases is an effective method of treatment of Eagle syndrome, that carries low risk of complications.
Źródło:
Polish Journal of Otolaryngology; 2019, 73, 5; 18-24
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Social Functioning of Women with Turner Syndrome
Autorzy:
Zadrożna, Ilona
Powiązania:
https://bibliotekanauki.pl/articles/918005.pdf
Data publikacji:
2013-01-01
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
social functioning
women
Turner syndrome
Opis:
The article concerns social functioning of women with Turner syndrome, focusing particularly on their family life (relations with parents, siblings, partner and children), and relations with others (friends, acquaintances, workmates and members of TS support organizations). The author also tries to find correlations between growth hormone treatment, sex hormones treatment, age of TS diagnosis, karyotype and social functioning of TS women. Turner Syndrome is a quite common (1 in every 2500 live female births) human genetic disorder which affects only females. Females with TS lack all or part of one of two sex X chromosomes. The phenotype of TS women includes short stature and ovarian failure (which usually causes infertility) specific anatomic abnormalities (such as a short neck with a webbed appearance, a low hairline at the back of the neck, and low-set ears) and characteristic neurocognitive profile, which usually does not include mental retardation. The treatment of TS girls includes growth hormone and sex hormones therapy. 71 women took part in the study (30 from Poland and 41 from other countries – USA, Australia and United Kingdom). Researches indicated that generally women with TS showed relatively good functioning in relations in family of origin (with parents and siblings) and in social environment (quite high professional activity, good functioning in relations with friends and acquaintances). Relations with parents, especially with mothers, were usually very close, but often revealed overprotective parents’ attitude towards TS women (even in their adult life). Relations with fathers were slightly worse, more often revealing lack of fathers’ acceptance towards TS women. Relations with siblings were rather close, but again revealed overprotective siblings’ attitude towards TS sisters. Researches also revealed relatively weak functioning of TS women in relations in family of procreation (with partner and children).
Źródło:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej; 2013, 1; 121-137
2300-391X
Pojawia się w:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Acute coronary syndrome in cancer patients. Part II: invasive and conservative treatment options, takotsubo syndrome problem
Autorzy:
Piotrowski, Grzegorz
Powiązania:
https://bibliotekanauki.pl/articles/1035854.pdf
Data publikacji:
2020-10-30
Wydawca:
Medical Education
Tematy:
acute coronary syndrome
cardio-oncology
treatment strategies
Opis:
Acute coronary syndrome (ACS) and oncological disease are more frequently observed in the general population as discussed in the part I of this article. Treatment of myocardial infarction in oncological patients becomes a real struggle for clinicians, especially that the data from clinical trials including cancer patients with ACS are very limited. The choice of treatment modality should consider many existing factors considering the type of ACS – non-ST-segment elevation myocardial infarction vs ST-segment elevation myocardial infarction, patient’s condition, type of cancer and oncological treatment applied. Taking into consideration above mentioned factors, clinicians have to face three therapeutic options: invasive, conservative or combination of both in order to choose the best and most beneficial treatment. This article summarizes the current therapeutic approach to the management of ACS in cancer patients.
Źródło:
OncoReview; 2020, 10, 3; 89-97
2450-6125
Pojawia się w:
OncoReview
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Iron in medicine and treatment
Żelazo w medycynie i lecznictwie
Autorzy:
Luchowska-Kocot, D.
Powiązania:
https://bibliotekanauki.pl/articles/13550.pdf
Data publikacji:
2014
Wydawca:
Uniwersytet Warmińsko-Mazurski w Olsztynie / Polskie Towarzystwo Magnezologiczne im. Prof. Juliana Aleksandrowicza
Tematy:
iron
medicine
treatment
iron deficiency
anaemia
restless legs syndrome
Willis-Ekbom disease zob.restless legs syndrome
Wittmaack-Ekbom syndrome zob.restless legs syndrome
pregnancy
Opis:
Being a component of many proteins and enzymes, iron is an essential microelement for humans. However, this element can also be toxic when present in excess because of its ability to generate reactive oxygen species. This dual nature imposes a strict regulation mechanism of the iron concentration in the body. In humans, systemic iron homeostasis is mainly regulated on the level of intestinal absorption. A patient diagnosed with excess iron in the body should be treated safely and effectively. And the therapy should be consistent with the treatment of concurrent diseases. On the other hand, iron deficiency is one of the most common disorders affecting humans. Iron-deficiency anaemia continues to represent a major public health problem worldwide, being prevalent among pregnant women, where it represents an important risk factor for maternal and infant health. A problem detecetd relatively recently and therefore not fully clarified yet is the iron therapy in patients with restless legs syndrome (RLS). RLS is a common neurological condition defined clinically as the urge to move the legs. Reduced brain iron is strongly associated with restless legs syndrome. RLS can also be a consequence of iron deficiency in the body. This review will focus on iron as an element whose abnormal metabolism or deficiency in the body can lead to diseases e.g. anaemia, restless legs syndrome and iron overload. Here we will describe methods of therapy, paying particular attention to the types and dosages of medications.
Żelazo jest podstawowym mikroelementem organizmu ludzkiego, stanowi bowiem istotny element wielu białek i enzymów. Jednak pierwiastek ten może wykazywać działanie toksyczne, gdy występuje w nadmiarze, ze względu na jego zdolność do generowania reaktywnych form tlenu. Ten podwójny charakter żelaza narzuca ścisłą regulację stężenia żelaza w organizmie. U ludzi homeostaza ustrojowa żelaza jest głównie regulowana na poziomie wchłaniania jelitowego. Pacjent, u którego zdiagnozowano nadmiar żelaza w organizmie, powinien być poddany bezpiecznemu i skutecznemu leczeniu, które jest zgodne z terapią współistniejących schorzeń. Niedobór żelaza jest jednym z najczęstszych zaburzeń dotykających ludzi. Niedokrwistość spowodowana niedoborem żelaza nadal stanowi istotny problem zdrowia publicznego na całym świecie. Szczególnie dotyczy kobiet w ciąży, stanowiąc istotny czynnik ryzyka dla zdrowia matki i dziecka. Stosunkowo nowym i nie do końca wyjaśnionym zagadnieniem jest terapia żelazem chorych na zespół niespokojnych nóg (RLS). Jest to stan neurologiczny klinicznie określany jako przymus poruszania nogami. Z zespołem niespokojnych nóg związana jest ściśle redukcja żelaza w mózgu. RLS może być również konsekwencją niedoboru żelaza w organizmie. W pracy omówiono nieprawidłowy metabolizm żelaza lub jego brak w organizmie, co może prowadzić do ww. jednostek chorobowych. Opisano również metody terapii, zwracając szczególną uwagę na rodzaj i wielkość dawki proponowanych leków.
Źródło:
Journal of Elementology; 2014, 19, 3
1644-2296
Pojawia się w:
Journal of Elementology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mothers of children with Tourette’s syndrome
Autorzy:
Khoury, Rita
Powiązania:
https://bibliotekanauki.pl/articles/937928.pdf
Data publikacji:
2018-09-09
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
Mothers
Tourette syndrome
Quality of Life
Opis:
The purpose of this study was to gather data from the mothers of children with Tourette Syndrome (TS), in order to examine the extent to which the existence of a child with TS in the family affected mothers’ Quality of Life (QOL). The research was conducted according to the qualitative methods. Data was collected from semistructures interviews with 50 mothers of children with TS. The interviews were analyzed using a content analysis method. Conclusions derived from the research findings found that lack of accurate diagnosis and information leaded mothers to a state of imbalance and great stress. When they were given accurate information, they seemed to be more able to advocate for the child with TS and thus preventmisunderstandings, and consequent unpleasant situations and confusion.
Źródło:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej; 2017, 19; 171-199
2300-391X
Pojawia się w:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Child with Down Syndrome in a peer group.
Autorzy:
Jędrzejowska, Agnieszka
Powiązania:
https://bibliotekanauki.pl/articles/941275.pdf
Data publikacji:
2019-12-15
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
peer group
Down syndrome
integration
Opis:
The attitude towards people with disabilities has changed over the last century. Both deinstitutionalisation as well as integration and normalisation allowed many people with intellectual disabilities to improve their social situation. An example of such a systemic solution supporting the development of disabled persons are integration groups. The subject of this article is a report from a pilot study on the functioning of a group of children with Down syndrome within an integration group. The objective of this study was the presentation of the reasonability of inclusion within the integration group of children with Down’s Syndrome (with the homogeneous dysfunction). Observation and sociometric tests covered children with Down syndrome from two integration groups from kindergarten no. 109 in Wrocław, Poland. I consider the essence of integration, following A. Maciarz, to be the feeling of social bonds experienced by a disabled individual, a sense of belonging to a group, as well as the conviction that one is accepted by it, despite the fact that the standards adopted by their community are not always and not fully met by them. The research was carried out for six months in a kindergarten where I was a special educator.
Źródło:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej; 2019, 27; 351-372
2300-391X
Pojawia się w:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Measuring the value of scientific achievements
Autorzy:
Drozdowicz, Zbigniew
Powiązania:
https://bibliotekanauki.pl/articles/704077.pdf
Data publikacji:
2019
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
bibliometrics
expert syndrome
point syndrome
impact factors
Opis:
In these considerations, I undertake a polemic with thinking based on the assumption that the value of scientific achievements can be measured with almost mathematical accuracy and give fully reliable point indicators for them. It is not only part of those who introduce the current reform of higher education and science in Poland, but also experts who support them, as well as some representatives of science and natural sciences. This thinking was called point syndrome and expert syndrome. Although it was diagnosed as a manifestation of academic disease a few years ago, it still not only finds its supporters, but also translates into activities, which in some scholars cause astonishment, in others indignation, and still strong opposition in others.
Źródło:
Nauka; 2019, 2
1231-8515
Pojawia się w:
Nauka
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Event-related potentials as an index of lost cognitive control and lost self in a TBI patient with duration increasing post-traumatic Delusional Misidentification Syndrome concluded with Cotard Syndrome
Autorzy:
Pąchalska, Maria
Powiązania:
https://bibliotekanauki.pl/articles/2106070.pdf
Data publikacji:
2019
Wydawca:
Fundacja Edukacji Medycznej, Promocji Zdrowia, Sztuki i Kultury Ars Medica
Tematy:
memory
working autobiographic memory
executive dysfunction
delusional misidentification syndromes
Cotard syndrome
Capgras syndrome
Fregoli syndrome
P300
N170
Opis:
The goal of the study was twofold: 1) to evaluate the QEEG/ ERPs indexes of functional brain impairment in a TBI patient diagnosed with chronic lost cognitive control and lost self caused by post traumatic, and here increasing over time, delusional misidentification syndrome concluded with Cotard syndrome in the blooming stage, with nihilistic delusions concerning the body and existence, and the delusion of being dead, and 2) to explore the mind of a patient whose identity has been disengaged, and who experiences the loss of his self and relations with his immediate surroundings with all the tragic consequences that entails. I herein present a 52-year-old patient, who – after a serious head injury due to a car accident 20 years ago, which re- sulted in focal injuries in the frontal and temporal areas of the right hemisphere – developed Cotard syndrome. After arousal from a 63-day coma and 98 days of post-traumatic amnesia, he manifested: (1) the loss of autobiographical memory, (2) a lost self, (3) forgotten family ties (including his lover). The study revealed that the patient’s cognitive control system is completely destroyed: no cognitive components have been found. Recall from memory has been completely disturbed (a low amplitude of N170). The two hemispheres work inco- herently with the right hemisphere revealing a serious delay in memory recall.
Źródło:
Acta Neuropsychologica; 2019, 17(4); 487-508
1730-7503
2084-4298
Pojawia się w:
Acta Neuropsychologica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Triple negative breast cancer with ACTH-dependent Cushings syndrome - case report
Autorzy:
Hodorowicz-Zaniewska, Diana
Brzuszkiewicz, Karolina
Szpor, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/1392214.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
breast cancer
paraneoplastic syndrome
ACTH
adrenocorticotropin
Cushing’s syndrome
Opis:
Introduction: Endocrine and metabolic paraneoplastic syndromes in the course of malignant tumors result from ectopic production of hormones or hormone precursors in tumor cells. Production of hormones by endocrine tumors is relatively frequent, while such production by adenocarcinoma cells is definitely rare. The study presents a case of triple-negative invasive breast cancer, with the ectopic secretion of ACTH (adrenocorticotropic hormone), which provokes serious metabolic disorders. Materials and methods: The patient was admitted to hospital with symptoms of Cushing`s syndrome. Diagnostic tests revealed that the cause of metabolic disorders was breast cancer. After proper preparation, the patient was qualified for surgery. Results: After the mastectomy, the patient’s metabolism stabilized. The patient underwent adjuvant chemotherapy and radiotherapy. Four months after the last cycle of systemic treatment, cancer dissemination was found. The patient was treated with second-line chemotherapy, however, control CT revealed progression. The patient died 20 months after surgery and two months after the last cycle of chemotherapy. Conclusions: The case reported in this study – triple-negative invasive breast cancer, responsible for ectopic production of ACTH and causing Cushing’s syndrome – is a rare phenomenon. Treatment of patients with breast cancer showing hormonal activity should not differ from general rules applied for breast cancer. However, due to accompanying metabolic disturbances, the patients need individualized oncological approach, precise diagnostic tests, and adequate preoperative preparation.
Źródło:
Polish Journal of Surgery; 2019, 91, 2; 45-47
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Skutki przemocy – zespół barona Münchhausena
Effects of violence – Munchhausen syndrome
Autorzy:
Żukowska-Nawrot, Karina
Powiązania:
https://bibliotekanauki.pl/articles/501377.pdf
Data publikacji:
2012
Wydawca:
Instytut Studiów Międzynarodowych i Edukacji Humanum
Tematy:
violence
Munchhausen syndrome
Opis:
Humanistic psychology assumes that a child is by nature good and noble, and what he will become in the future depends on the kind of environment where the processes of upbringing and socialisation have taken place. Violence is beyond any doubt a social phenomenon which does not have any moral, territorial, or religious borders. Experiencing violence in childhood often determines undertaking destructive behaviours by an individual.
Źródło:
Społeczeństwo i Edukacja. Międzynarodowe Studia Humanistyczne; 2012, 2(10); 215-218
1898-0171
Pojawia się w:
Społeczeństwo i Edukacja. Międzynarodowe Studia Humanistyczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Physiotherapeutic management of a patient with patellofemoral pain syndrome – a case report
Autorzy:
Ustarbowska, Katarzyna
Trybulec, Bartosz
Powiązania:
https://bibliotekanauki.pl/articles/454991.pdf
Data publikacji:
2018
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
patellofemoral pain syndrome excessive lateral pressure syndrome
runner’s knee
physiotherapy
kinesiotaping
Opis:
Introduction. Patellofemoral pain syndrome (PFPS) is a disorder of the front compartment of the knee joint with incompletely investigated, probably multifactorial pathogenesis. It mostly affects young people and runners. In patients with PFPS conservative management is a therapy of choice with fundamental importance of physiotherapeutic procedures. Therapy should be highly individualized and considering all possible factors that may cause PFPS symptoms. Aim. The aim of this report was presentation of management of a 23 year old female patient with PFPS that developed secondary to a knee sprain. The medical history, diagnostic and therapeutic procedures were thoroughly described, then obtained results were presented and thereafter discussed. Methods. Clinical assessment included functional and provocative tests of the patellofemoral joint as well as thigh and calf muscles tests, range of motion measurement of the knee joint and pain assessment using the VAS scale. Therapeutic management included 5 sessions of post-isometric muscle relaxation (PIR), mobilizations of the patella and applications of elastic tapes. Results. After 5 sessions of therapeutic management PFPS symptoms were significantly reduced. Pain did not occur during normal activity, whereas in heavy joint loading, it occurred later and was of lower intensity. Range of motion as well as subjective sense of joint stability was also improved. Conclusions. Individually adjusted conservative management based on PIR techniques, mobilizations of patella and kinesiotaping seems to be effective form of therapy for PFPS of functional nature
Źródło:
European Journal of Clinical and Experimental Medicine; 2018, 1; 68-75
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Syndrom poobozowy (KZ Syndrome)
Syndrome de la vie après le camp de concentration (KZ Syndrom)
Autorzy:
Leszczyński, Stanisław Z.
Powiązania:
https://bibliotekanauki.pl/articles/502789.pdf
Data publikacji:
1996
Wydawca:
Wyższe Seminarium Duchowne w Łodzi
Źródło:
Łódzkie Studia Teologiczne; 1996, 5; 295-300
1231-1634
Pojawia się w:
Łódzkie Studia Teologiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The bilaterality of idiopathic carpal tunnel syndrome among manual workers
Autorzy:
Lewańska, Magdalena
Powiązania:
https://bibliotekanauki.pl/articles/2116642.pdf
Data publikacji:
2020-03-13
Wydawca:
Instytut Medycyny Pracy im. prof. dra Jerzego Nofera w Łodzi
Tematy:
syndrome
CTS
idiopathic
tunnel
carpal
bilaterality
Opis:
ObjectivesTo evaluate: a) the prevalence of bilateral idiopathic carpal tunnel syndrome (CTS) in manual workers; b) a correlation between the duration of unilateral and bilateral CTS symptoms; c) a correlation between the onset of CTS symptoms in the unilateral dominant/non-dominant hand and the time of developing bilateral CTS; and d) findings of the nerve conduction study (NCS) in symptomatic and asymptomatic hands of patients with unilateral CTS.Material and MethodsClinical and neurophysiological examinations were conducted along with a detailed analysis of job exposure of 332 manual workers admitted to the Occupational Medicine Department, the Nofer Institute of Occupational Medicine, with suspected occupational CTS. Eventually, 258 patients were excluded from the study: 34 with associated neuropathies and 206 with other conditions potentially associated with CTS. Cases with work-related CTS (18) were also excluded.ResultsA total of 74 patients were diagnosed as idiopathic CTS. In idiopathic CTS, the right hand was affected in 15 (20.3%) patients, the left hand in 4 (5.4%) patients, and both hands in 55 (74.3%) patients. Symptoms duration was longer in the patients with bilateral CTS (4.01 years) than in those with a unilateral right (1.7 years, p = 0.002) or left hand condition (2.8 years, p = 0.313). Median nerve impairment at the wrist was revealed by NCS in 6 left and 2 right asymptomatic hands.ConclusionsThe findings of the study indicate the need for “alerting” patients with unilateral CTS about the risk of the disease developing in the contralateral hand. Therefore, NCS should be routinely performed in the asymptomatic hands of patients with unilateral CTS, which is essential for the prevention of neuropathies, especially among manual workers performing repetitive manual tasks.
Źródło:
International Journal of Occupational Medicine and Environmental Health; 2020, 33, 2; 151-161
1232-1087
1896-494X
Pojawia się w:
International Journal of Occupational Medicine and Environmental Health
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Sjögrens syndrom – the review of the latest diagnostic guidelines essential for otolaryngologists
Autorzy:
Kruk, Karolina
Rzepakowska, Anna
Osuch-Wójcikiewicz, Ewa
Niemczyk, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1399442.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
autoimmune sialadenitis
dry mouth
dryness syndrome
sicca syndrome
Sjögren syndrome
Opis:
Sjogren’s syndrome (SS) is a complex connective tissue disease with autoimmune background and high clinical, radiological and molecular heterogeneity. SS is typically manifested by sicca syndrome, characterized by dry eyes and dry mouth due to autoimmune-induced inflammation of the lacrimal and salivary glands. Complications of sicca syndrome are dental caries, oral candidiasis, dysosmia, dysgeusia, difficulties in swallowing and chewing. SS may coexist with other diseases of rheumatoid and autoimmune etiology. SS is linked to an 16-fold increased risk of non-Hodgkin lymphoma. Early diagnosis results in appropriate treatment and may slow down the course of the disease and limit extraglandular involvement. Due to diverse clinical phenotypes and symptomatology, establishing of the diagnosis is often difficult. In 2016 the AmericanEuropean Consensus Group (AECG) and European League Against Rheumatism (EULAR) proposed a classification system that defines SS as a systemic disease. Diagnostic tools in establishing SS diagnosis are serological tests, ultrasonography, Schirmer’s test, unstimulated whole saliva flow rate and Ocular Staining Score. The complete curing of SS is still not possible. As a complex multisystem disease, SS requires multidisciplinary cooperation and individual diagnostic and therapeutic approaches in patients. Therapy is focused on the treatment of symptoms and prophylaxis of complications. The laryngological treatment of oral cavity symptoms in SS include supervision of proper oral hygiene habits and adequate fluids supplementation. The EULAR Sjögren’s syndrome disease activity index (ESSDAI) and Clinical Oral Dryness Score(CODS) are used to monitor disease progression and treatment effectiveness.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2019, 8, 2; 1-6
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The Loser Syndrome – universality of the strategy of defense of discriminated groups
Autorzy:
Pospiszyl, Irena
Powiązania:
https://bibliotekanauki.pl/articles/1365374.pdf
Data publikacji:
2020-11-01
Wydawca:
Fundacja Pedagogium
Tematy:
victims
loser syndrome
oppressive situation
social minority
symptoms of the loser syndrome
humiliation
scapegoat
long-term oppressive situation
Opis:
If one assumes, like Mayer Hacker, that a  social minority is a  group of people who, because of their physical or cultural characteristics, are not treated as equal to other groups in a  given society, then it turns out that many groups meet these criteria. In the prison subculture they are met by „losers,” in the macro-social space – by all minority groups such as national, ethnic, racial minorities, but also women and some religious minorities. It is surprising that although these groups often have comparable numerical, physical, or intellectual strength to that of the mainstream group, they are unable to obtain equal treatment, respect, and all the privileges that this entails. This is probably due to a number of factors, including tradition, cultural capital, resources, and culturally established institutions promoting specific social groups. However, an equally important determinant is the own activity of individuals forming a minority group, and their ability to integrate and consolidate with their own group. Among others, the following contribute to this: lack of intra-group solidarity, orientation towards the dominant group, excessive guilt, contempt for one’s own group etc. The article deals with the barriers inherent in the minority groups themselves, which contribute significantly to the consolidation of their unfavorable status. The size and scale of these barriers contribute to the status that I  call the loser syndrome. It is also important that the factors limiting the expansion of minority groups are similar in most minority groups. They are characterized by a certain universality.
Źródło:
Resocjalizacja Polska; 2020, 19; 91-108
2081-3767
2392-2656
Pojawia się w:
Resocjalizacja Polska
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The Loser Syndrome – universality of the strategy of defense of discriminated groups
Autorzy:
Pospiszyl, Irena
Powiązania:
https://bibliotekanauki.pl/articles/1365371.pdf
Data publikacji:
2020-12-29
Wydawca:
Fundacja Pedagogium
Tematy:
victims
loser syndrome
oppressive situation
social minority
symptoms of the loser syndrome
humiliation
scapegoat
long-term oppressive situation
Opis:
If one assumes, like Mayer Hacker, that a  social minority is a  group of people who, because of their physical or cultural characteristics, are not treated as equal to other groups in a  given society, then it turns out that many groups meet these criteria. In the prison subculture they are met by „losers,” in the macro-social space – by all minority groups such as national, ethnic, racial minorities, but also women and some religious minorities. It is surprising that although these groups often have comparable numerical, physical, or intellectual strength to that of the mainstream group, they are unable to obtain equal treatment, respect, and all the privileges that this entails. This is probably due to a number of factors, including tradition, cultural capital, resources, and culturally established institutions promoting specific social groups. However, an equally important determinant is the own activity of individuals forming a minority group, and their ability to integrate and consolidate with their own group. Among others, the following contribute to this: lack of intra-group solidarity, orientation towards the dominant group, excessive guilt, contempt for one’s own group etc. The article deals with the barriers inherent in the minority groups themselves, which contribute significantly to the consolidation of their unfavorable status. The size and scale of these barriers contribute to the status that I  call the loser syndrome. It is also important that the factors limiting the expansion of minority groups are similar in most minority groups. They are characterized by a certain universality.
Źródło:
Resocjalizacja Polska; 2020, 20; 91-108
2081-3767
2392-2656
Pojawia się w:
Resocjalizacja Polska
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
DOES GERSTMANN SYNDROME EXIST?
Autorzy:
Pyrtek, Sylwia
Badziński, Arkadiusz
Adamczyk-Sowa, Monika
Pąchalska, Maria
Powiązania:
https://bibliotekanauki.pl/articles/2137819.pdf
Data publikacji:
2020-05-14
Wydawca:
Fundacja Edukacji Medycznej, Promocji Zdrowia, Sztuki i Kultury Ars Medica
Tematy:
brain damage
Gerstmann syndrome
neuropsychological deficit
Opis:
The aim of the study is to present Gerstmann syndrome, manifested as a neuropsychological deficit resulting from the damage to the parietal lobe of the left hemisphere. Here it is discussed based on the studies conducted mainly since the 1950’s when it attracted considerable interest, as well as and controversy at the same time. The classic symptoms are briefly described, including the clinical tasks useful in any the diagnosis for during the neuropsychological assessment. The paper also presents recent studies and a alternative different proposal for the understanding of this clinical syndrome. Josef Gerstmann described a clinical tetrad in his patients, which was later to be known as Gerstmann syndrome. The symptoms included finger agnosia, agraphia, acalculia and left-right disorientation. He associated the above symptoms with damage to the left angular gyrus, hence the alternative a different name for of the syndrome i.e., the angular gyrus syndrome. The existence of the syndrome was questioned for some time, something which was never approved by Gerstmann. Currently, the occurrence of the syndrome is confirmed by studies. However, the full and pure tetrad of the classic symptoms as observed is not common. The clinical picture of the syndrome often usually remains incomplete and is related to other neuropsychological deficits such as aphasia, which frequently occurs. In modern considerations, the language deficiencies of semantic aphasia are not treated as non- Gerstmann syndrome, disturbing its pure form, but are considered to be a part of Gerstmann syndrome as such.
Źródło:
Acta Neuropsychologica; 2020, 18(2); 259-284
1730-7503
2084-4298
Pojawia się w:
Acta Neuropsychologica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Carpenter syndrome: cone beam computed tomography pictorial review
Syndrome de Carpenter: revue illustrée utilisant la tomodensitométrie volumique à faisceau conique.
Autorzy:
Delroisse, Adrien
Olszewski, Raphael
Powiązania:
https://bibliotekanauki.pl/articles/2129099.pdf
Data publikacji:
2022-04-03
Wydawca:
Presses Universitaires de Louvain
Tematy:
Carpenter syndrome
CBCT
oligodontia
acrocephalopolysyndactyly type II
single solitary lower incisor
syndrome de Carpenter
acrocéphalopolysyndactylie type II
oligodontie
incisive centrale unique solitaire
Opis:
Objective: To describe dentoalveolar findings in one pediatric patient with a very rare Carpenter syndrome or acrocephalopolysyndactyly type II, and using cone beam computed tomography (CBCT). Case report: We found a syndromic oligodontia, upper canine transmigration, and an exceptional agenesis of four lateral incisors. We also described the fourth case in the literature of a single solitary lower incisor on the midline, and the first case ever illustrated on CBCT. Conclusions: We proposed and illustrated the use of the system of progressive numbering of teeth on CBCT axial views to better understand complex dental clinical situations such as syndromic oligodontia.
Objectifs de travail: Evaluer la région dento-alvéolaire chez un patient pédiatrique atteint d'un très rare syndrome de Carpenter ou d'acrocéphalopolysyndactylie de type II à l'aide de la tomodensitométrie volumique à faisceau conique (CBCT). Cas clinique: Nous avons retrouvé une oligodontie syndromique, une transmigration canine supérieure et une agénésie exceptionnelle des quatre incisives latérales. Nous avons également décrit le quatrième cas dans la littérature d'une seule incisive inférieure solitaire sur la ligne médiane, et le premier cas jamais illustré sur CBCT. Conclusions: Nous avons proposé et illustré l'utilisation du système de numérotation progressive des dents sur des vues axiales CBCT pour mieux comprendre les situations cliniques dentaires complexes telles que l'oligodontie syndromique.
Źródło:
Nemesis. Negative Effects in Medical Sciences Oral and Maxillofacial Surgery; 2022, 22, 1; 1-15
2593-3604
Pojawia się w:
Nemesis. Negative Effects in Medical Sciences Oral and Maxillofacial Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Evaluation Of Irritable Bowel Syndrome Symptoms Amongst Warsaw University Students
Autorzy:
Niemyjska, Sylwia
Ukleja, Anna
Ławiński, Michał
Powiązania:
https://bibliotekanauki.pl/articles/1395637.pdf
Data publikacji:
2015-05-01
Wydawca:
Index Copernicus International
Tematy:
irritable bowel syndrome
IBS
Opis:
Irritable bowel syndrome (IBS) belongs to functional gastrointestinal disorders and is characterized by abdominal pain and change in stool consistency and/or bowel habits. Etiological factors include gastrointestinal peristalsis disturbances, visceral hypersensitivity, chronic inflammation of the mucous membrane, dysbacteremia, intestinal infections, psychosomatic and nutritional factors. Gastrointestinal motility disturbances in case of IBS are manifested by the inhibition of the intestinal passage, which favors the development of constipation or occurrence of diarrhea. The aim of the study was to evaluate IBS symptoms and demonstrate the relationship between physical activity and place of residence amongst Warsaw University students. Material and methods. The study was conducted in march, 2014 using a specific questionnaire, amongst Warsaw University students. The study group comprised 120 female patients, aged between 19 and 27 years (M=23.43; SD=1.29). The chi-square test was used for analysis, p<0.05 was considered as statistically significant. Results. The BMI of investigated patients ranged between 16.30-31.22 kg/m2 (M=21.27; SD=2.71). The majority of respondents (76.6%) weighed within the normal limits. Abdominal pain or discomfort occurred more frequently in the group of students who considered their physical activity as low. In case of respondents with a low physical activity bowel movement disorders and stool continence changes occurred more often, as compared to those with moderate physical activity. The most common symptom was rectal tenesmus, the least common-presence of mucous in the stool. Analysis showed that students with low physical activity were more frequently absent from school/work, due to abdominal symptoms. The respondents with moderate activity more often considered their abdominal symptoms, being associated with stress. Conclusions. IBS symptoms are common amongst Warsaw University students. In case of respondents with low physical activity, abdominal pain or discomfort occurred more often. It has been demonstrated that diet and stress might contribute to the occurrence of abdominal symptoms, being evidence of IBS.
Źródło:
Polish Journal of Surgery; 2015, 87, 5; 252-259
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Guillain-Barre syndrome as a paraneoplastic syndrome in a 17-year- old boy
Zespół Guillain-Barre jako zespół paranowotworowy u 17-letniego chłopca
Autorzy:
Dryżałowski, Paweł
Sołowiej, Elżbieta
Okruciński, Damian
Jóźwiak, Sergiusz
Powiązania:
https://bibliotekanauki.pl/articles/1836001.pdf
Data publikacji:
2020
Wydawca:
Polskie Towarzystwo Neurologów Dziecięcych
Tematy:
Guillain-Barre syndrome
hodgkin lymphoma
paraneoplastic syndrome
polyneuropathy
demyelination
Zespół Guillain-Barre
chłoniak hodgkina
zespół paranowotworowy
polineuropatia
demielinizacja
Opis:
Guillain-Barre syndrome (GBS) is an acute inflammatory polyneuropathy, characterised by progressive, symmetrical muscle weakness and sensory disorder due to autoimmunologic myelin nerve sheats and/or peripheral nerves axonal damage. The course of the disease in children is usually milder than in adults. The most common variant of GBS is acute inflammatory demyelinating polyneuropathy (AIDP). GBS is a rare disorder with morbidity rate of 0,5-1,5/100 000/ year, more often seen in males. The course of disease in children is usually milder than in adults. Early diagnosis and proper treatment enables complete recovery in 80% of cases, while approximately 10% of patients suffer from symptoms recurrence, mainly after infection. Almost 2/3 of GBS cases are preceded by upper respiratory or gastrointestinal infection. The emergence of antibodies in various mechanisms, which cross react with nerve sheats or axon antigens (through a phenomenon known as molecular mimicry), leads to development of the syndrome. Known triggers inducing GBS include viral and bacterial infections, injuries, surgery, bone marrow transplantation and rarely childhood vaccinations. In still rarer cases, GBS may develop in the course of paraneoplastic syndrome (PNS), and be the first symptom of an underlying neoplastic process.
Zespół Guillain-Barre (GBS) jest ostrą zapalną polineuropatią, charakteryzującą się postępującym, symetrycznym osłabieniem mięśni i zaburzeniami czuciowymi, wynikającymi z autoimmunologicznego uszkodzenia osłonek mielinowych nerwów i/lub uszkodzenia aksonalnego nerwów obwodowych. Najczęstszym rodzajem GBS jest ostra zapalna polineuropatia demielinizacyjna (AIDP). GBS to rzadkie schorzenie o współczynniku zachorowalności 0,5– 1,5 / 100 000 / rok, częściej obserwowane u mężczyzn. Przebieg choroby u dzieci jest zwykle łagodniejszy niż u dorosłych. Wczesna diagnoza i odpowiednie leczenie umożliwiają całkowite wyleczenie w 80% przypadków. Około 10% pacjentów cierpi na nawrót objawów, głównie po zakażeniu. Wielu pacjentów skarży się na przetrwałe zmęczenie. Niewydolność oddechową obserwuje się u 10–20%, a zgon występuje w 3–5% wszystkich przypadków. Prawie 2/3 przypadków GBS poprzedzone jest infekcją górnych dróg oddechowych lub przewodu pokarmowego. Pojawienie się w różnych mechanizmach przeciwciał, które reagują krzyżowo z osłonkami nerwów lub antygenami aksonów (poprzez zjawisko zwane mimikrą molekularną), prowadzi do rozwoju zespołu. Pośród czynników wywołujących GBS, wymienić można te związane ze szczepieniami, urazami lub przeszczepem szpiku kostnego. GBS może być także zespołem paraneoplastycznym (PNS), często obserwowanym jako jako pierwszy objaw procesu nowotworowego.
Źródło:
Neurologia Dziecięca; 2020, 29, 58; 86-88
1230-3690
2451-1897
Pojawia się w:
Neurologia Dziecięca
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Wolf–Hirschhorn syndrome – a case report
Zespół Wolfa–Hirschhorna – opis przypadku
Autorzy:
Bulak, Halyna
Kopanska, Dzwenyslava
Powiązania:
https://bibliotekanauki.pl/articles/1034426.pdf
Data publikacji:
2017
Wydawca:
Medical Communications
Tematy:
Wolf–Hirschhorn syndrome
hypertelorism
microcephaly
micrognathia
Opis:
Wolf–Hirschhorn syndrome is a severe genetic condition that affects many systems of the human body. The genetic mechanism is based on the deletion of the distal portion of the short arm of chromosome 4 (4p). Individuals affected by the syndrome have a special phenotype: wide bridge of the nose, widely spaced eyes, micrognathia, microcephaly, growth retardation, cryptorchidism, heart defects, hearing loss and severe intellectual disability. The patient from our case report was hospitalised at the Lviv City Children’s Hospital at the age of six hours in a severe condition, with distinctive features of a genetic syndrome, which was connected with intraventricular haemorrhage. At the age of three months, he showed delayed physical and neurocognitive development and a characteristic appearance, which led to a specialist consultation to diagnose the genetic disease. This time, on the basis of clinical, laboratory and instrumental findings, the boy was diagnosed with Wolf–Hirschhorn syndrome.
Zespół Wolfa–Hirschhorna jest ciężką chorobą genetyczną objawiającą się szeregiem wad wrodzonych dotykających różnych układów ludzkiego organizmu. Mechanizm genetyczny tego zespołu polega na delecji dystalnej części krótkiego ramienia chromosomu 4 (4p). Osoby dotknięte tym schorzeniem mają charakterystyczny fenotyp, na który składają się m.in. szeroka podstawa nosa, szeroko rozstawione oczy, mikrognacja, mikrocefalia, upośledzenie wzrostu, wnętrostwo, wady serca, ubytki słuchu oraz ciężkie upośledzenie intelektualne. Przedstawiony w pracy pacjent był hospitalizowany w Miejskim Szpitalu Dziecięcym we Lwowie w 6. godzinie życia w stanie ciężkim, z wyraźnymi cechami zespołu zaburzeń genetycznych oraz krwawieniem dokomorowym. W wieku 3 miesięcy, ze względu na wyraźnie opóźniony rozwój motoryczny oraz neuropoznawczy, a także charakterystyczne cechy fizjonomiczne, pacjenta skierowano do konsultacji genetycznej w celu ustalenia rozpoznania. W oparciu o wyniki badań fizykalnych, laboratoryjnych i genetycznych stwierdzono u niego zespół Wolfa–Hirschhorna.
Źródło:
Pediatria i Medycyna Rodzinna; 2017, 13, 2; 267-269
1734-1531
2451-0742
Pojawia się w:
Pediatria i Medycyna Rodzinna
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Prevention and nutritional therapy of metabolic syndrome
Autorzy:
Rożniata, M.
Zujko, K.
Zujko, M.E.
Powiązania:
https://bibliotekanauki.pl/articles/1918547.pdf
Data publikacji:
2018-01-09
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
metabolic syndrome
obesity
blood pressure
dyslipidemia
hyperglycemia
Opis:
The term metabolic syndrome (MetS) defines the cooccurrence of the related risk factors of metabolic origin that promote the development of cardiovascular diseases with atherosclerotic background and type 2 diabetes. The diagnostic criteria of MetS have undergone modifications for years. Until now no clear definition of MetS has been established. The latest diagnostic criteria of MetS published in 2009 by a group of IDF (International Diabetes Federation) and AHA/NHLBI (American Heart Association/ National Heart, Lung and Blood Institute) experts discern three out of five risk factors: abdominal obesity (taking into consideration population differences), elevated level of triglycerides, reduced HDL cholesterol, hypertension and fasting hyperglycemia. Genetic predispositions and environmental factors, such as lack of physical activity and improper diet are considered to be responsible for MetS development. Therefore, prevention and treatment of MetS should be based first of all on a change in modifiable lifestyle factors, among which proper diet is of essential importance.
Źródło:
Progress in Health Sciences; 2017, 7(2); 100-104
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Burnout syndrome in male and female gestalt and cognitive-behavioral psychotherapists
Autorzy:
Rzeszutek, Marcin
Powiązania:
https://bibliotekanauki.pl/articles/2128378.pdf
Data publikacji:
2019-04-04
Wydawca:
Katolicki Uniwersytet Lubelski Jana Pawła II. Towarzystwo Naukowe KUL
Tematy:
burnout syndrome
gender
Gestalt psychotherapy
cognitive-behavioral psychotherapy
Opis:
The objective of this article is to investigate gender differences in the level of professional burnout among male and female Gestalt and cognitive-behavioral psychotherapists according to the length of professional experience as a covariate. The study was conducted on 200 participants: 100 Gestalt psychotherapists and 100 cognitive-behavioral psychotherapists. The results show a positive relationship between the length of professional experience and the level of burnout in the whole group of psychotherapists. Additionally, it has been shown that the level of burnout in the male psychotherapists’ group was significantly higher than the intensity of symptoms in the female group. The difference in the intensity of burnout symptoms between the Gestalt therapists and cognitive behavioral therapists was not statistically significant.
Źródło:
Roczniki Psychologiczne; 2013, 16, 1; 155-161
1507-7888
Pojawia się w:
Roczniki Psychologiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bodybuilding links to Upper Crossed Syndrome
Autorzy:
Daneshmandi, Hasan
Harati, Javad
Fahim Poor, Saeid
Powiązania:
https://bibliotekanauki.pl/articles/1031755.pdf
Data publikacji:
2017
Wydawca:
PPHU Projack Jacek Wąsik
Tematy:
abnormality
bodybuilders
forward head posture
upper crossed syndrome
Opis:
Introduction: Upper cross syndrome is becoming more prevalent in today’s population. The syndrome is described as a postural disorder presenting with over active pectoralis musculature and upper trapezius musculature. Also there is inhibition of lower and middle trapezius musculature, which results in winging of scapula, elevated and abducted scapula. This scapular dyskinesia, per se, resulted in rounding of shoulders. The syndrome is often associated with bad posture in routine life or occupation of a person. Little is known about the relationship between sport participation and postural body changes of bodybuilding training. Our aim is to investigate whether bodybuilding training in trained-individuals is associated with the postural abnormalities in the upper body. Methods: 60 male, trained bodybuilders (age= 24.62±3.67 years, body weight= 82.40±9 kg, height= 175±0.067 cm, body mass index (BMI( = 26.77±2.37 Kg/m2, body fat percentage = 21.58±3.21) and 30 un-trained (age= 24.67±2.24 years, body weight= 73.33±9.42 kg, height= 175±0.06 cm, body mass index (BMI) = 23.93±3.16 Kg/m2, body fat percentage = 18.17±3.76) volunteered and were thus included in the study. Postural photographs were taken in the sagittal and frontal planes, and were analyzed by using AutoCAD software. The Flexi curve ruler was used for the assessment of thoracic kyphosis and lumbar lordosis. Results: Using an independent sample t-test, significant differences were observed in the values of forward head posture between trained and untrained groups (p=0.001) and Mann-Whitney U test showed there was significant differences between the values of uneven shoulders (p=0.001), rounded shoulder (p=0.009) and kyphosis (p=0.013), but there was no significant difference between lordosis values in two groups. Conclusion: It can be concluded that there is a high incidence of upper body abnormalities among bodybuilders and this should be taken as a minatory situation on behalf of bodybuilding trainers. Therefore, strength coaches should design an appropriate training program to prevent their trainees from such abnormalities.
Źródło:
Physical Activity Review; 2017, 5; 124-131
2300-5076
Pojawia się w:
Physical Activity Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Post-transplant Metabolic Syndrome (PTMS) after Liver Transplantation – Review of the Literature
Autorzy:
Kotarska, Katarzyna
Raszeja-Wyszomirska, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/1054740.pdf
Data publikacji:
2015
Wydawca:
Uniwersytet Szczeciński. Wydawnictwo Naukowe Uniwersytetu Szczecińskiego
Tematy:
liver transplantation
metabolic syndrome
Opis:
Liver transplant provides a definitive therapeutic measure for patients with chronic and acute liver diseases. Apart from the improvement of overall health, an organ transplant entails several metabolic complications. They are multi-agent and depend, among others, on the function of organ being transplanted, adverse effects of immunosuppression being applied, organ complications induced by failure of the organ being transplanted, current treatment, concomitant diseases and consequences of the acute and chronic rejection processes. Improvements in surgical techniques, peritransplant intensive care, and immunosuppressive regimens have resulted in significant improvements in short-term survival. Focus has now shifted to address long-term outcomes of liver transplantation. Therefore, this paper presents the current review of literature referring to specificity of the prevalence of metabolic syndrome and its complications in patients after liver transplantation.
Źródło:
Central European Journal of Sport Sciences and Medicine; 2015, 11, 3; 29-37
2300-9705
2353-2807
Pojawia się w:
Central European Journal of Sport Sciences and Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Prevalence of metabolic syndrome in normal weight individuals
Autorzy:
Suliga, Edyta
Kozieł, Dorota
Głuszek, Stanisław
Powiązania:
https://bibliotekanauki.pl/articles/989634.pdf
Data publikacji:
2016
Wydawca:
Instytut Medycyny Wsi
Tematy:
metabolic syndrome
risk factors
body mass index
Opis:
Introduction and objective. The prevalence of metabolic syndrome and overweight in individuals with normal body weight is connected with higher exposure to type 2 diabetes and cardiovascular diseases. The aim of the study was to evaluate the risk and frequency of occurrence of metabolic syndrome and each of its components among individuals with normal weight. Materials and method. Data were obtained by structured interview, and by measurements of anthropometric factors and blood analyses among 13,172 individuals aged 37–66. The risk of occurrence of metabolic syndrome was analysed in tertiles within the normal range of BMI (18.5–24.9 kg/m2). Results. Metabolic syndrome was diagnosed in 17.27% of individuals with normal weight. A significant increase in the risk of occurrence of metabolic syndrome in females was observed within the second (OR = 2.22; 95% CI: 1.63–3.05) and the third (OR = 3.97; 95% CI: 2.97–5.36) tertiles of normal BMI values. In males, a significantly higher risk of occurrence of metabolic syndrome was noted only in the highest BMI tertile (OR = 2.16; 95% CI: 1.26–3.83), compared to the reference level. Conclusions. A high frequency of occurrence of metabolic syndrome risk factors was observed among individuals with BMI close to the upper cut-off point of the normal range. In order to early diagnose metabolically obese individuals with normal weight it is necessary to check the waist circumference when BMI ≥ 22.5 kg/m2 in females, and BMI ≥ 23.8 kg/m2 in males, where abnormal values should be a signal that further examinations should be performed to determine other risk factors of metabolic syndrome.
Źródło:
Annals of Agricultural and Environmental Medicine; 2016, 23, 4
1232-1966
Pojawia się w:
Annals of Agricultural and Environmental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
An Analysis of Identity Construction in Interactional Narratives by Women with Turner Syndrome
Autorzy:
Ciepiela, Kamila
Powiązania:
https://bibliotekanauki.pl/articles/1368410.pdf
Data publikacji:
2020-12-30
Wydawca:
Uniwersytet Łódzki. Wydawnictwo Uniwersytetu Łódzkiego
Tematy:
identity
interview
narrative
positioning
Turner syndrome
Opis:
The study aims to uncover and explore the social identities of women suffering from a genetic disorder called Turner syndrome (TS), and whose main symptoms are a short stature and gonadal dysgenesis. Such a genetically-determined physical appearance is argued to influence the positioning of TS women in the web of social relationships and identities. This linguistic analysis of narratives delivered by Polish women with TS in semi-structured interviews aims to explicate the extent to which they are actors or recipients in creating their own identities. The analysis draws on the assumptions of the ‘small story’ paradigm developed by Michael Bamberg (1997, 2005) who claims that in interaction, narrative is not only used to convey meaning, but also to construct the identities of the interlocutors. Thus, narrative is treated in a functional way, in which its formal structure and content are integrally associated with its use and any deviations are relativized as a consequence of a user’s deliberate activity.
Źródło:
Research in Language; 2020, 18, 4; 407-420
1731-7533
Pojawia się w:
Research in Language
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Sleep duration and metabolic syndrome
Autorzy:
Kawada, Tomoyuki
Powiązania:
https://bibliotekanauki.pl/articles/2168365.pdf
Data publikacji:
2016-11-18
Wydawca:
Instytut Medycyny Pracy im. prof. dra Jerzego Nofera w Łodzi
Tematy:
short sleep duration
long sleep duration
metabolic syndrome
cross-sectional study
sex difference
causality
Źródło:
International Journal of Occupational Medicine and Environmental Health; 2016, 29, 6; 877-878
1232-1087
1896-494X
Pojawia się w:
International Journal of Occupational Medicine and Environmental Health
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Hereditary mixed polyposis syndrome –- own experience
Autorzy:
Kamocki, Zbigniew
Piłaszewicz, Agata
Zaręba, Konrad
Powiązania:
https://bibliotekanauki.pl/articles/1394430.pdf
Data publikacji:
2012
Wydawca:
Index Copernicus International
Tematy:
hereditary mixed polyposis syndrome
HMPS
colorectal cancer
surgical treatment
Opis:
Hereditary mixed polyposis syndrome (HMPS) is a rare condition of unknown genetic origin. The paper presents 25-year clinical follow up in a female patient with multiple gastrointestinal tract polyps of varied histology. They most likely served as sites of multiple colorectal cancers development. The clinical course is interesting in terms of diagnostics and therapy. The patient required extended genetic testing, intensive conservative treatment and numerous surgical procedures. This is the first case of HMPS presented in Polish publications.
Źródło:
Polish Journal of Surgery; 2012, 84, 5; 262-266
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Środowisko szkoły w narracjach uczniów z zespołem Aspergera – wnioski z badań
School environment in the Asperger Syndrome students narration, research conclusions
Autorzy:
Moszyńska, Małgorzata
Powiązania:
https://bibliotekanauki.pl/articles/1371188.pdf
Data publikacji:
2018-09-09
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
Asperger Syndrome
mass education of disabled students
narration of students with Asperger Syndrome
Opis:
The article addresses the subject of social functioning of a student diagnosed with Asperger Syndrome in the environment of a mass education school, in his subjective opinion. Methodologically speaking it is based on qualitative studies and the aim of the research was to reach subjective significance given by the students with Asperger Syndrome to this institution and understanding the role it plays for them.
Źródło:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej; 2017, 19; 167-176
2300-391X
Pojawia się w:
Interdyscyplinarne Konteksty Pedagogiki Specjalnej
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Post intensive care syndrome prevention and impact of COVID 19
Autorzy:
Alefragkis, Dimitrios
Powiązania:
https://bibliotekanauki.pl/articles/1918959.pdf
Data publikacji:
2021-06-14
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
COVID 19
post intensive care syndrome
intensive care unit
prevention
Opis:
In recent years, there has been a maximum increase in admissions to the intensive care unit, culminating in an exponential increase in admissions during the COVID 19 pandemic. Many patients who survived and were discharged from the intensive care unit have cognitive, physical, and psychological disorders that are reflected in the term post-intensive care syndrome. Patients and their families show symptoms of anxiety, depression, post-traumatic stress, and sleep problems. The result is that they negatively affect their quality of life. Numerous risk factors contribute to the development of this syndrome, mainly the sedation, the duration of mechanical ventilation, and the length of stay in the intensive care unit. For this reason, it is necessary to take measures to prevent this syndrome including ABCDEFGH care plan, physical rehabilitation, nutritional support, and intensive care unit diaries. Care must also be given to the creation of Post Intensive care unit clinics where they have a diagnostic, therapeutic, counseling, and rehabilitation role that will act as assistants in the care of patients after discharge from the intensive care unit. Also, special care should be taken with patients who have recovered from COVID 19 whose needs are increasing and need immediate treatment. This review aims to analyze post-intensive care syndrome, prevention measures, and the impact of COVID 19. In conclusion, it is necessary to take measures to treat post-intensive care unit syndrome with early diagnosis and treatment, to reduce the adverse effects on both patients and their families.
Źródło:
Progress in Health Sciences; 2021, 11(1); 112-117
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Ramsay Hunt syndrome with deep hearing loss and meningitis
Autorzy:
Błochowiak, Katarzyna
Kamiński, Bartłomiej
Powiązania:
https://bibliotekanauki.pl/articles/454755.pdf
Data publikacji:
2018
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
s. facial palsy
hearing loss
meningitis
Ramsay Hunt syndrome
Opis:
Introduction. Ramsay Hunt syndrome is a clinical manifestation of varicella zoster virus reactivation. It is characterized by an erythematous vesicular rash in the external auditory canal and pinna with otalgia, vertigo and ipsilesional facial palsy. Symptoms develop over a few days with prodromal signs of facial weakness, tingling, facial numbness. Usually, cranial nerves VII and VIII are involved in the inflammatory process. Possible consequences of Ramsay Hunt syndrome are hearing loss, encephalitis and meningitis. Description of the case report. The authors present the case of a 63-year-old woman with a vesicular rash, earache, vertigo and left-sided facial paralysis who was treated with antiviral drugs and analgesics. These symptoms were complicated by conductive hearing loss in the left ear and meningitis. After treatment facial paralysis decreased. Unfortunately, hearing loss was permanent. Discussion. Rapid administration of antivirals and corticosteroids limited facial paralysis and improved facial expression. The prognosis for facial palsy is poorer in Ramsay Hunt syndrome than in idiopathic forms. Conclusions. A past history of vertigo and hypertension could been a predisposing factor for the severe manifestation of Ramsay Hunt syndrome and subsequent complications
Źródło:
European Journal of Clinical and Experimental Medicine; 2018, 1; 60-62
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Münchhausenov syndrómv zastúpení v kontexte psychiatrických diagnóz
Autorzy:
Ďurkovský, Peter
Powiązania:
https://bibliotekanauki.pl/articles/2141354.pdf
Data publikacji:
2011
Wydawca:
Instytut Studiów Międzynarodowych i Edukacji Humanum
Tematy:
Anamnesis
Child abuse and neglect syndrome
Münchhausen syndrome by proxy
Social work
Violence
Opis:
Münchhausen syndrome by proxy is keeping back form of child abuse and neglect syndrome. Everyone keeps silent about it. Charitable professions keep silent about it too. Lot of charitable professions dont ́ have scientific foundation. Child is victim for parents and charitable professions. Disclousure of Münchhausen syndrome by proxy menace for lot of people. They are afraid of unemployment.
Źródło:
Humanum. Międzynarodowe Studia Społeczno-Humanistyczne; 2011, 1(6); 193-198
1898-8431
Pojawia się w:
Humanum. Międzynarodowe Studia Społeczno-Humanistyczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Current recommendations for treatment and diagnosing of xerostomia in Sjögren’s syndrome
Autorzy:
Zablotskyy, Oleh
Tomczyk, Martyna
Błochowiak, Katarzyna
Powiązania:
https://bibliotekanauki.pl/articles/454735.pdf
Data publikacji:
2019
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
saliv
Sjögren syndrome
xerostomia
Opis:
Introduction. Xerostomia is one of the most common and disturbing adverse effects of systemic diseases and their therapies. This complication markedly increases the risk for dental caries, difficulties with chewing, swallowing and sleep disorders with a significant impact on the patient’s quality of life. Sjögren’s syndrome (SS) is a systemic autoimmune disease that primarily affects the exocrine glands, resulting in dryness of the mouth due to lymphocytic infiltration of the salivary glands. Aim. The aim of this paper is to present the current recommendations in diagnosing and treating SS-related xerostomia. Material and methods. Analysis of literature Results. For the assessment of SS-related xerostomia, only an unstimulated salivary flow with rates of 0.1 mL/min is included in the current SS classification criteria. Saxon test, sialography, ultrasonography of salivary glands play supporting function. Treatment of SS -related xerostomia includes an application of secretagogues and the implementation of specific dental prophylaxis measures. Adjuvant therapies include herbal remedies, photobiomodulation, and acupuncture. Conclusion. Treatment of SS requires multidisciplinary care. There is no fully effective treatment of xerostomia that provides immediate and long-lasting results.
Źródło:
European Journal of Clinical and Experimental Medicine; 2019, 4; 356-363
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Specifics of mental disorders of patients with metabolic syndrome
Autorzy:
Kleban, K. I.
Powiązania:
https://bibliotekanauki.pl/articles/765439.pdf
Data publikacji:
2017
Wydawca:
Uniwersytet Mikołaja Kopernika w Toruniu. Wydział Nauk o Ziemi i Gospodarki Przestrzennej. Katedra Kultury Fizycznej
Tematy:
nonpsychotic mental disorders, psychosomatic disorders, metabolic syndrome, desynchronosis, chronobiological processes
Opis:
In the general-somatic network there is a steady increase in the number of patients with psychosomatic disorders. Problems of providing adequate psychiatric and psychotherapeutic assistance to this category of patients are related to the motivation of patients to participate in psychological measures and the readiness of the medical system to provide comprehensive care on the basis of the biopsychosocial approach. Mental factors are involved both in the occurrence and course of a metabolic syndrome in the form of a patient's lifestyle and behavior patterns of healthy functioning, and is a consequence of somatic pathology. Mental factors are involved both in the occurrence and course of a metabolic syndrome in the form of a patient's lifestyle and behavior patterns of healthy functioning, and is a consequence of somatic pathology. So mental disorders of metabolic syndrome are manifested in the form of psychosocial maladaptation, neurotic, affective, personality, and organic disorders. Desynchronosis which is a factor of the development of a metabolic syndrome and characterizes the complex chronobiological component of the regulation of psychophysiological functions in norm and under the influence of stress, deserves special attention.Addressing the diagnosis of mental disorders associated with metabolic syndrome is precisely aimed at determining chronobiological disorders of psychosomatic integrated areas and is supposed to improve diagnostic and treatment process and to shorten the treatment of these disorders.
Źródło:
Journal of Education, Health and Sport; 2017, 7, 9
2391-8306
Pojawia się w:
Journal of Education, Health and Sport
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Christophe Jaffrelot, Le syndrome pakistanais, Fayard, Paris 2013, str. 657
Christophe Jaffrelot, Le syndrome pakistanais, Fayard, Paris 2013, pp. 657
Autorzy:
Burakowski, Adam
Powiązania:
https://bibliotekanauki.pl/articles/961625.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Orientalistyczne
Źródło:
Przegląd Orientalistyczny; 2014, 3-4; 211-212
0033-2283
Pojawia się w:
Przegląd Orientalistyczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The Body Discourse and Dystopian Identity Narratives of Women with Turner Syndrome
Autorzy:
Ciepiela, Kamila
Powiązania:
https://bibliotekanauki.pl/articles/971258.pdf
Data publikacji:
2020
Wydawca:
Łódzkie Towarzystwo Naukowe
Tematy:
Turner syndrome
discourse analysis
dystopia
identity
narrative
positioning
Opis:
The aim of the article is to compare and contrast dystopian discourse with the first-person life narratives told by females with a rare genetic disorder, Turner syndrome (TS). Employing the methodology of discourse analysis, I trace the themes related to the most challenging areas of the lives of women with TS, and find certain tendencies in the way they position themselves and others in the contemporary discourse of medical treatment, femininity and social relationships. I analyze stories whose characters are developed on the basis of experiences that their tellers lived through. I argue that the discourse of Turner syndrome and the dystopian discourse are analogous on the grounds of the rarity of the syndrome and its two main symptoms - short stature and gonadal dysgenesis.
Źródło:
Zagadnienia Rodzajów Literackich; 2020, 63, 1; 63-74
0084-4446
Pojawia się w:
Zagadnienia Rodzajów Literackich
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Partial remission in patient with Richter syndrome: an „emergency” treatment with pixantrone
Autorzy:
Szwedyk, Paweł
Powiązania:
https://bibliotekanauki.pl/articles/1035640.pdf
Data publikacji:
2020-06-30
Wydawca:
Medical Education
Tematy:
Richter syndrome
chemotherapy
chronic lymphocytic leukemia
immunotherapy
pixantrone
Opis:
Chronic lymphocytic leukemia is the most commonly recognized type of leukemia in adults. The appearance of systemic symptoms such as weight loss, fever, or local symptoms in the form of rapidly growing organomegaly, lymphadenopathy in a patient with CLL raises the suspicion of transformation into a high-grade lymphoma – defined as Richter syndrome which is usually associated with very poor prognosis. The described case concerns a 71-year-old patient with this diagnosis, in whom due to the confirmed resistance to subsequent lines of immuno- and chemotherapy, an „emergency” treatment with a modern chemotherapy drug from the aza-anthracendion group – pixantrone was used. Treatment with pixantrone was associated with a relatively good response, translating into partial remission (also in the area of infiltrative changes in the head and neck structures), stabilization of the course of the disease and, consequently, allowed to extend the patient’s life.
Źródło:
OncoReview; 2020, 10, 2; 52-56
2450-6125
Pojawia się w:
OncoReview
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quantitative assessment of nutrition in patients with polycystic ovary syndrome (PCOS)
Autorzy:
Szczuko, M.
Skowronek, M.
Zapalowska-Chwyc, M.
Starczewski, A.
Powiązania:
https://bibliotekanauki.pl/articles/877679.pdf
Data publikacji:
2016
Wydawca:
Narodowy Instytut Zdrowia Publicznego. Państwowy Zakład Higieny
Tematy:
quantitative assessment
human nutrition
patient
diet
nutrient
nutrition deficiency
polycystic ovary syndrome
PCOS zob.polycystic ovary syndrome
Opis:
Background. PCOS (polycystic ovary syndrome) is called a pathology of the XX century and affects at least 10-15% women of childbearing age. The therapy involves pharmacotherapy of hormonal imbalance, as well as the change of lifestyle, including the diet. Objective. Performing the quantitative assessment of components of diets of women with PCOS, comparing the results with current dietary standards for Polish people and defining dietary requirements for the patients. Material and Methods. The study was performed on 54 women of childbearing age (average age 26.03± 5.52) with PCOS syndrome diagnosed according to on the Rotterdam criteria. Anthropometric measurements of the patients were made and BMI and WHR calculated. Quantitative assessment of women’s diets was performed based on the analysis of 3-day food diaries and food records taken from the previous 24h with the interview method. The data were introduced to a dietary software DIETA 5.0, calculating the average intake of the energy, nutrients, vitamins, minerals, cholesterol and dietary fibre. The obtained results were compared to Polish dietary guidelines. Results. Examined group was characterized by increased waist circumference (98.71± 13.6 cm) and an average WHR was 0.92± 0.08. An increased average value of BMI was also shown (28.91± 5.54 kg/m2). The patients consumed, on average, 1952.5±472.7 kcal daily, and the risk of insufficient intake of protein was determined in 36.7% of examined women. The highest risk of deficiency in minerals in women with PCOS was related to calcium (634 mg), potassium (3493 mg) and magnesium (250.1 mg), whereas with reference to vitamins deficiency as much as 70% of tested women were at risk of insufficient intake of folic acid, 36.7% of them - vitamin C, and 26.7% - vitamin B12. The average consumption of vitamin D was at the level of 3.4 μg. Test group was characterized by excessive average consumption of total fat (50%), SFA (70.4%) and saccharose (50%). The percentage of people with excessive average intake of cholesterol was at the level of 40.74%. As much as 83.3% patients consumed too low amounts of dietary fibre in their diets (<25g). Conclusions. In diet therapy of women with PCOS there should be higher intake of folic acid, vitamins D and C, cobalamin, dietary fibre and calcium. The consumption of total fats, saturated fatty acids and cholesterol should be reduced, as through facilitating the development of diabetes and cardio-vascular diseases, they affect the dysfunction of ovaries. The diet of some of the patients should be also supplemented by potassium, magnesium and zinc. The introduction of a properly balanced diet should be the key in the treatment of women with PCOS diagnosed according to Rotterdam criteria.
Wstęp. Syndrom policystycznych jajników (PCOS) nazywany jest patologią XX wieku i dotyka co najmniej 10–15% kobiet w wieku reprodukcyjnym. Terapia dotyczy zarówno leczenia farmakologicznego zaburzeń hormonalnych, metabolicznych jak również zmiany stylu życia, w tym sposobu żywienia. Cel. Ocena składu ilościowego jadłospisów kobiet z PCOS, porównanie go z obowiązującymi normami żywienia dla ludności polskiej oraz sprecyzowanie zaleceń żywieniowych dla pacjentek. Materiał i metody. Badaniami objęto 54 kobiety w wieku rozrodczym, z rozpoznanym, według kryteriów Rotterdamskich, zespołem PCO (średni wiek to 26,03± 5,52 lat). Wykonano pomiary antropometryczne oraz obliczono wskaźniki BMI i WHR. Oceny ilościowej sposobu żywienia kobiet dokonano w oparciu o analizę trzydniowych dzienniczków oraz jadłospisu zebranego metodą wywiadu o spożyciu z ostatnich 24 godzin. Dane wprowadzono do programu dietetycznego DIETA 5.0, obliczając średnią podaż energii, składników odżywczych, witamin, składników mineralnych, cholesterolu oraz błonnika. Uzyskane wyniki porównano z obowiązującymi w Polsce normami żywienia. Wyniki. Badana grupa charakteryzowała się zwiększonym obwodem pasa 98,71± 13,6 cm, a średnia WHR była równa 0,92± 0,08. Wykazano zwiększoną średnią wartość wskaźnika BMI (28,91± 5,54 kg/m2). Pacjentki spożywały średnio 1952,5±472,7 kcal dziennie, a zagrożenie niedostatecznym spożyciem białka stwierdzono u 36,7% badanych kobiet. Największe ryzyko wystąpienia deficytu składników mineralnych u kobiet z PCOS dotyczyło wapnia (634 mg), potasu (3493mg), magnezu (250,1 mg) natomiast wśród witamin aż 70% kobiet badanych było zagrożonych niewystarczającym spożyciem folianów, 36,7% niedoborem witaminy C a 26,7% witaminą B12. Średnie spożycie witaminy D kształtowało się na poziomie 3,4 μg. Badana grupa charakteryzowała się nadmiernym średnim spożyciem tłuszczu ogółem (50%) NKT (70.4%) i sacharozy (50%). Odsetek osób z nadmiernym średnim poborem cholesterolu był na poziomie 40.74%. Aż 83.3% pacjentek miało zbyt niską podaż błonnika w diecie (<25g). Wnioski. W dietoterapii kobiet z PCOS należy zwiększyć podaż folianów, witaminy D i C, kobalaminy, błonnika oraz wapnia. Powinno ograniczyć się spożycie tłuszczu ogółem, nasyconych kwasów tłuszczowych i cholesterolu które pogłębiając rozwój cukrzycy i chorób sercowo-naczyniowych wpływają na dysfunkcję jajnika. Dietę części pacjentek z PCOS należałoby również uzupełnić w potas, magnez, cynk. Wprowadzenie prawidłowo zbilansowanej diety powinno być kluczem w leczeniu kobiet z PCOS rozpoznawanych kryteriami Rotterdamskimi.
Źródło:
Roczniki Państwowego Zakładu Higieny; 2016, 67, 4
0035-7715
Pojawia się w:
Roczniki Państwowego Zakładu Higieny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Second branchial cleft fistula in a child with genetically confirmed branchio-oto-renal (BOR) syndrome
Autorzy:
Remjasz, Agnieszka
Clarós, Pedro
Powiązania:
https://bibliotekanauki.pl/articles/1399630.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
second branchial cleft fistula
branchio-oto-renal syndrome
BOR syndrome
ear malformation
neck fistula
neck surgery
genetic disorders
Opis:
Preface: Branchial cleft anomalies constitute 32% to 45% of all neck pathologies in the pediatric population. These disorders may be a part of a branchio-oto-renal (BOR) syndrome, characterized by branchial arch abnormalities, preauricular pits, hearing impairment, and various types of renal disorders. Usually, the treatment of a branchial fistula does not necessarily require extensive diagnostics before the treatment. However, in some cases, branchial cleft fistulas may occur together with other congenital disorders. A case report: The aim of this study is to present diagnostic and therapeutic difficulties in a 4-year old male patient with a complete second branchial cleft fistula and additional congenital, bilateral hearing loss. The course of the disease, diagnostic difficulties, and its treatment are presented. Genetic counseling finally confirmed the mutation of an EYA1 gene, responsible for the occurrence of BOR syndrome. The child undergone a total fistula resection without any complications during hospitalization or in the postoperative treatment. Summary: Presentation of this clinical case was intended primarily to remind that such defects may occur in the association with other anomalies, for example, deafness or renal disorders. When dealing with such patients, it is worth paying attention to the detailed examination and diagnostics, including genetic counseling, hearing tests or abdominal ultrasound. Special radiological imaging should also be performed in case of the unusual course of the fistula or probable proximity to vital structures, what is essential during qualification for surgery. Finally, we wanted to describe alternative methods of treatment for the standard surgical technique that may be used in a selected group of patients.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2019, 8, 1; 63-70
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Przeniesiony zespół Münchausena – sposoby indukowania objawów chorobowych u dzieci
Methods of disease symptom induction in Münchausen syndrome by proxy
Autorzy:
Janus, Tomasz
Powiązania:
https://bibliotekanauki.pl/articles/499316.pdf
Data publikacji:
2015
Wydawca:
Fundacja Dajemy Dzieciom Siłę
Tematy:
przeniesiony zespół Münchausena
zaburzenia pozorowane
zespół dziecka maltretowanego
Münchausen syndrome by proxy
factitious disorders
battered child syndrome
Opis:
Przeniesiony zespół Münchausena został opisany w 1977 roku przez brytyjskiego pediatrę Roya Meadowa w artykule Munchausen syndrome by proxy. The hinterland of child abuse. Autor opisał dwa przypadki intencjonalnego manipulowania wywiadem chorobowym, a także fabrykowania wyników badań diagnostycznych przez opiekuna w celu wzbudzenia u personelu medycznego podejrzenia choroby somatycznej dziecka. W artykule Meadow podkreślał, że poszukiwanie przez lekarzy źródła przyczyn objawów chorobowych występujących u dzieci wiązało się z wieloma potencjalnie szkodliwymi procedurami diagnostyczno-terapeutycznymi, w tym zabiegami przeprowadzonymi w trzech różnych ośrodkach klinicznych. Jedno dziecko, przewlekle zatruwane solą kuchenną przez matkę, zmarło. W niniejszym artykule przeanalizowano wykorzystywane przez opiekunów metody intencjonalnie pogorszające stan zdrowia dziecka w celu poddania go procedurom diagnostycznym i leczniczym. Do analizy włączono 68 artykułów, zarówno polskich, jak i zagranicznych, zawierających opisy 100 przypadków przeniesionego zespołu Münchausena. W analizie wykazano, że opiekunowie mogą stosować różnorodne, często wymyślne i bardzo złożone sposoby indukowania objawów chorobowych, a jedynymi ograniczeniami wydają się być są motywacja, fantazja, wiedza i doświadczenie sprawcy.
Münchausen Syndrome by Proxy was described in 1977 by British pediatrician, Roy Meadow. In the article “Munchausen syndrome by proxy. The hinterland of child abuse” Meadow presented two cases of disease symptom induction in children done by the biological mother. The author drew attention to the phenomenon of intentional manipulation of medical history, as well as fabricating the results of diagnostic tests by the caregiver in order to arouse suspicion of a child’s somatic illness in medical staff. In his article Meadow emphasizes that diagnostic and therapeutic efforts have been associated with numerous potentially harmful procedures, including surgeries in three different clinical centers. One child, chronically intoxicated with salt by his mother, died. Since the first publication about Munchausen Syndrome by Proxy many similar cases have been described in Polish and world literature. The aim of this paper is to analyze the methods which caregivers use to intentionally worsen their children’s health in order to force medical staff to perform diagnostic and therapeutic procedures. Analysis of 68 articles containing descriptions of 100 Munchausen syndrome by proxy cases was conducted. Analysis has shown that caregivers can use various and elaborate methods of disease symptom induction which may be limited by motivation, ingenuity, knowledge and perpetrators’ experience only.
Źródło:
Dziecko krzywdzone. Teoria, badania, praktyka; 2015, 14, 3; 9-37
1644-6526
Pojawia się w:
Dziecko krzywdzone. Teoria, badania, praktyka
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Chronic cough: new concepts and therapeutic possibilities
Autorzy:
Arcimowicz, Magdalenia
Niemczyk, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1401753.pdf
Data publikacji:
2016
Wydawca:
Index Copernicus International
Tematy:
cough
chronic cough
upper airway cough syndrome
Cough Hypersensitivity Syndrome
diagnosis
therapy
Opis:
Cough is the most common symptom of the upper and lower airway diseases. In its nature, cough is a defence re-flex mechanism of the respiratory tract that is used to clear the upper and lower airways. Chronic cough, defined as cough lasting for more than 8 weeks, is reported in 3–40% of the general population and has an important impact on patients’ quality of life, by causing anxiety, physical discomfort, social isolation and personal emabarrassment, be-ing an often medical complaint and one of the most common reasons for outpatient visits. Upper airway cough syn-drome, asthma, eosinophilic bronchitis and gastroesophageal reflux diseases account for most chronic cough after excluding somking, angiotensin-converting enzyme inhibitor use and chronic bronchitis. Many patients have more than one reason for chronic cough. Some complex diagnostic procedures, in many individuals are necessary to rec-ognized the cause/causes of chronic cough and to establish the accurate diagnosis, which implies a higher chance of effective treatment. Despite detailed diagnostic procedures, in many cases, the efficacy of chronic cough treatment is questionable and ambiguous. We observe not always satisfactory response to therapy. There are some coughs that seem refractory despite an extensive work-up. The possibility of hypersenitive cough reflex response, defining pa-tients with Cough Hypersensitivity Syndrome has been proposed to explain these cases, rather resistant to cough treatment, previously known as idioapthic cough or refractory, unexplained cough. The concept of Cough Hypersen-sitivity Syndrome helps us to understand the mechanisms underlying cough and provides better therapeutic options to treat chronic cough, like neuromodulating drugs, and speech therapy.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2016, 5, 1; 22-29
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Spektrum płodowych zaburzeń alkoholowych (FASD – fetal alcohol syndrome disorder)
Fetal alcohol syndrome disorder (FASD)
Autorzy:
Nowak, Anna
Michno, Adrian
Powiązania:
https://bibliotekanauki.pl/articles/2082478.pdf
Data publikacji:
2019-12-31
Wydawca:
Państwowa Wyższa Szkoła Techniczno-Ekonomiczna im. ks. Bronisława Markiewicza w Jarosławiu
Tematy:
FAS
pregnancy
alcohol
ciąża
alkohol
Opis:
Spożywanie alkoholu w trakcie ciąży jest zjawiskiem wysoce niepożądanym, często powodującym poronienia lub wiele nieprawidłowości rozwojowych dziecka. Spektrum Płodowych Zaburzeń Alkoholowych, tzw. FASD (ang. Fetal Alcohol Spectrum Disorder) określa zaburzenia fizyczne i psychiczne wynikające z wpływu alkoholu na zdrowie oraz zaburzenia behawioralne dziecka, które zazwyczaj są wtórne do zmian zachodzących w ośrodkowym układzie nerwowym, wywołanych alkoholowym zatruciem płodu w trakcie ciąży. Zmiany te są zazwyczaj nieodwracalne i uwidaczniają się w trakcie całego życia dziecka dotkniętego FASD, ale dzięki odpowiednim terapiom istnieje możliwość zminimalizowania objawów tych zaburzeń. Ich charakter i ciężkość zależą od kilku czynników, między innymi od czasu ekspozycji na alkohol oraz stanu zdrowia kobiety ciężarnej. Wśród klinicznych cech FASD wyróżnia się anomalie w obrębie twarzoczaszki, zaburzenia ośrodkowego układu nerwowego oraz opóźnienie wzrostu. Zmiany strukturalne indukowane alkoholem obejmują anomalie w układzie sercowo-naczyniowym, szkieletowym, nerkowo-moczowodowym, a także w narządach wzroku i słuchu. Ważną rolę odgrywa czas postawienia wstępnej diagnozy, bowiem umożliwia on wprowadzenie odpowiedniej terapii dla dziecka z FASD oraz wprowadzenie odpowiedniej edukacji rodziców i rodziny chorego dziecka. Istnieje możliwość zminimalizowania objawów i zaburzeń wynikających ze Spektrum Płodowych Zaburzeń Alkoholowych, do stopnia umożliwiającego prawidłowe funkcjonowanie dziecka i jego rodziny.
Consumption of alcohol during pregnancy is a highly undesirable phenomenon, often causing miscarriages or many abnormalities of the child’s development. Fetal Alcohol Spectrum Disorder (FASD) describes physical and mental disorders resulting from the effects of alcohol on health and behavioral disorders of the child, which are usually secondary to changes in the central nervous system caused by fetal alcohol intoxication during pregnancy. These changes are usually irreversible and evident throughout the life of a child affected by FASD, but if appropriate therapies are implemented, it is possible to minimize the symptoms of these disorders. Their nature and severity depend on several factors, including the time of exposure to alcohol and the health status of a pregnant woman. Clinical features of FASD include craniofacial anomalies, central nervous system disorders and growth retardation. Alcohol-induced structural changes include anomalies in the cardiovascular, skeletal, renal and urinary systems as well as in the organs of sight and hearing. Time of initial diagnosis plays an important role, because it allows the introduction of appropriate therapy for a child with FASD and the introduction of appropriate education of parents and other members of the family. It is possible to minimize the symptoms and disorders resulting from the Fetal Alcohol Disorders Spectrum, to the extent that would enable proper functioning of the child and his family altogether.
Źródło:
Edukacja • Terapia • Opieka; 2019, 1; 114-128
2658-0071
2720-2429
Pojawia się w:
Edukacja • Terapia • Opieka
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Labial salivary gland biopsy in the diagnosis of Sjögren’s syndrome
Autorzy:
Błochowiak, Katarzyna
Sokalski, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/454844.pdf
Data publikacji:
2019
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
biopsy
labial glands
salivary glands
Sjögren’s syndrome
Opis:
Introduction. Labial salivary gland biopsy is used for diagnosis of Sjögren’s syndrome (SS) and lymphoma accompanying SS. Aim. The aim of this study was to present the main techniques used for taking labial salivary gland biopsies in the diagnosis of SS with respect to their advantages, histologic criteria, validation, complications, and their usefulness for diagnostic procedures, monitoring disease progression, and treatment evaluation. Material and methods. This study is based on analysis of literature. Results. The microscopic confirmation of SS is based on the presence of focal lymphocytic sialadenitis (FLS) with a focus score ≥1 per 4 mm2 of glandular tissue. A lymphocytic focus is defined as a dense aggregate of 50 or more lymphocytes adjacent to normal-appearing mucous acini in salivary gland lobules that lacked ductal dilatation. Other histopathological features of SS are lymphoepithelial lesions and a relative decrease of <70% IgA + plasma cells. Labial salivary gland biopsy is characterized by high specificity, a positive predictive value, and an average sensitivity of 79% in SS. Conclusion. It can be also valuable in diagnosing B-cell mucosa-associated lymphoid tissue (MALT) lymphomas but it is not recommended for the monitoring of SS progression and the effectiveness of the treatment. Persistent lower lip hypoesthesia is the most severe complication of labial salivary gland biopsy.
Źródło:
European Journal of Clinical and Experimental Medicine; 2019, 2; 162-168
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of ESWT in post-operative treatment in Carpal Tunnel Syndrome – a review
Autorzy:
Ambroziak, Maciej
Powiązania:
https://bibliotekanauki.pl/articles/1391699.pdf
Data publikacji:
2020
Wydawca:
Index Copernicus International
Tematy:
carpal tunnel syndrome
ESWT
post-operative treatment
rehabilitation
Opis:
The aim of this study is to evaluate the potential use of extracorporeal shockwave therapy (ESWT) in the post-operative treatment of patients with carpal tunnel syndrome. A body of evidence validates the use of ESWT in various medical areas, mostly in nephrolithiasis, but also in a number of musculoskeletal conditions and in wound healing. Our knowledge about the use of ESWT in carpal tunnel syndrome seems sparse, which combined with a lack of reference values, forms a major limitation of the use of ESWT in this condition.
Źródło:
Polish Journal of Surgery; 2020, 92, 3; 39-43
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Carpal Tunnel Syndrome in Occupational Medicine Practice
Autorzy:
Bugajska, J.
Jędryka-Góral, A.
Sudoł-Szopińska, I.
Tomczykiewicz, K.
Powiązania:
https://bibliotekanauki.pl/articles/90882.pdf
Data publikacji:
2007
Wydawca:
Centralny Instytut Ochrony Pracy
Tematy:
carpal tunnel syndrome
diagnostic methods
occupational medicine
Opis:
Work-related overload syndromes are chiefly associated with the upper limbs, where carpal tunnel syndrome (CTS) plays a leading role. This article analyses methods of diagnosing CTS, with special emphasis on those that can be used by physicians in early diagnosis of CTS in workers doing monotonous work. It also discusses occupational (e.g., assembly work, typing, playing instruments, packaging and work associated with the use of a hammer or pruning scissors) and extra-occupational factors (e.g., post-traumatic deformation of bone elements of the carpal tunnel, degenerative and inflammatory changes in tendon sheaths, connective tissue hypertrophy or formation of crystal deposits) leading to CTS; diagnostic methods (subjective symptoms, physical examination, manual provocative tests, vibration perception threshold, electrophysiological examination and imaging methods); and therapeutic and preventive management tools accessible in occupational medicine practice.
Źródło:
International Journal of Occupational Safety and Ergonomics; 2007, 13, 1; 29-38
1080-3548
Pojawia się w:
International Journal of Occupational Safety and Ergonomics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Opieka nad kobietą i dzieckiem z zespołem FAS
Care of woman and child of FAS syndrome
Autorzy:
Komorowska, Agnieszka
Powiązania:
https://bibliotekanauki.pl/articles/1029972.pdf
Data publikacji:
2018
Wydawca:
Państwowa Uczelnia Zawodowa we Włocławku
Tematy:
fetal alcohol syndrome
care
child
mother
Opis:
FAS- Fetal Alcohol Syndrome - is a disease consisting in neurobehavioral incorrectness as well as some changes in internal organs. This incorrectness occur at these children whose mothers drank alcohol during pregnancy. The FAS-children, apart from numerous changes in a body build, have problems with notice concentration, communication, incompetence of solving problems as well as with a weak impulse control. Their growing difficulties result from injury to Central Nerve system. Implementation of prophylaxis for the women is very important. It has in view to limit drinking alcohol by the pregnant women. The prenatal care of the pregnant women and her child is carried on by specialist health service centre and anti-alcoholic clinics. My work aimed at representing and trating defects that occur at these children whose mothers drank alcohol during pregnancy. The representing of methods of prophylaxis for the alcohol drinking women and trating a post – natal care of the mother and her child was a very important element of the paper.
FAS czyli Płodowy Zespół Poalkoholowy to jednostka chorobowa obejmująca nieprawidłowości neurobehawioralne oraz zmiany w organach wewnętrznych. Nieprawidłowości te występują u dzieci, których matki spożywały alkohol w okresie ciąży. Dzieci z FAS oprócz licznych zmian w budowie ciała mają problemy z koncentracją uwagi, komunikowaniem się, nieumiejętnością rozwiązywania problemów oraz ze słabą kontrolą impulsów. Trudności rozwojowe, jakie występują u tych dzieci wynikają z powodu uszkodzenia Ośrodkowego Układu Nerwowego. Bardzo ważnym elementem jest wdrażanie profilaktyki wśród kobiet, która ma na celu ograniczenie spożywania alkoholu przez kobiety ciężarne. Opieka perinatalna nad kobietą ciężarną powinna być już prowadzona przed ciążą oraz podczas porodu. Natomiast opieka poporodowa nad kobietą i jej dzieckiem powinna mieć na celu zapewnienie kontaktów z ośrodkiem specjalistycznym i poradnictwem antyalkoholowym. Celem pracy było przedstawienie i omówienie problemów związanych ze spożywaniem alkoholu przez kobiety ciężarne oraz omówienie wad, jakie występują u dzieci, których matki spożywały alkohol w okresie ciąży. Kolejnym ważnym aspektem było przedstawienie metod profilaktyki wśród kobiet spożywających alkohol oraz omówienie opieki okołoporodowej nad matką i jej dzieckiem.
Źródło:
Innowacje w Pielęgniarstwie i Naukach o Zdrowiu; 2018, 3, 2; 131-142
2451-1846
Pojawia się w:
Innowacje w Pielęgniarstwie i Naukach o Zdrowiu
Dostawca treści:
Biblioteka Nauki
Artykuł

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