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Wyświetlanie 1-2 z 2
Tytuł:
Life-threatening laryngeal attacks in hereditary angioedema patients
Autorzy:
Piotrowicz-Wójcik, Katarzyna
Porebski, Grzegorz
Powiązania:
https://bibliotekanauki.pl/articles/1397492.pdf
Data publikacji:
2020
Wydawca:
Index Copernicus International
Tematy:
C1 inhibitor
hereditary angioedema
icatibant
laryngeal attacks
Opis:
Background: Hereditary angioedema due to C1-inhibitor deficiency (HAE-C1INH) is a rare genetic disease that runs in the family. As a result of the disease, acute swellings of the subcutaneous tissue and mucous membranes of the digestive and respiratory systems, including the larynx, occur. Any attack of the disease involving the throat and larynx is particularly dangerous and requires knowledge of clinical determinants of the disease and its proper management.Materials and methods: The study included adult consecutive HAE-C1INH patients having follow-up visits in our centre. The group was examined with a structured clinical questionnaire, concerning the last 6 months and focusing particularly on laryngeal swelling attacks. Results: 55 subjects (F/M – 35/20, age range – 18–76) were included in the study. Laryngeal attacks occurred in 19 individuals (34.5%): 1–3, 4–6, and ≥7 attacks in 9, 8 and 2 patients, respectively, two of whom required intubation. In comparison to other patients, subjects with laryngeal attacks were characterised by significantly more frequent: (1) facial attacks, (2) severe disease activity, (3) the occurrence of female patients, (4) mental stress as a trigger of attacks. All patients with laryngeal attacks had a rescue medication at home and 15/19 (78%) patients could use it at home. Most of them used plasma-derived C1-inhibitor 17/19 (89.5%) and icatibant, 8/19 (42.1%). Discussion: HAE-C1INH patients with laryngeal attacks require particular attention. Proper training regarding the identifica-tion of these patients, adequate management, access to emergency services and emergency drugs are essential to ensure the safety of subjects with this localization of HAE-C1INH attacks
Źródło:
Polish Journal of Otolaryngology; 2020, 74, 2; 42-46
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
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
    Wyświetlanie 1-2 z 2

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