- Tytuł:
- A child with a rare genetic disease - Noonan syndrome
- Autorzy:
-
Siwik, P.
Janas, A. - Powiązania:
- https://bibliotekanauki.pl/articles/3700.pdf
- Data publikacji:
- 2015
- Wydawca:
- Instytut Medycyny Wsi
- Tematy:
-
child
human disease
rare disease
genetic disease
Noonan syndrome
autosomal dominant congenital disorder
surgical treatment - Opis:
- Noonan syndrome is a congenital developmental disorder characterized by short stature, facial dysmorphia, congenital heart defects and skeletal anomalies, with as estimated incidence of between one per 1000 and one per 2500 live births. The aim of our study is to present a case of dental surgical treatment of a child with such disorder. It is widely reported that children with mental disabilities receive less dental and medical care than their nondisabled counterparts. Because of this problem, it seems justified to describe the procedures of treating such children with dental issues, basing on a case of a girl with Noonan Syndrome.
- 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