Nonclassical Congenital Adrenal Hyperplasia and Pregnancy

Objective. The most common form of congenital adrenal hyperplasia (CAH) is 21-hydroxylase (21-OH) deficiency due to mutation of the CYP21A2 gene. Patients with nonclassical CAH (NC-CAH) are usually asymptomatic at birth and typically present in late childhood, adolescence, or adulthood with symptoms...

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Detalles Bibliográficos
Autores principales: Cuhaci, Neslihan, Aydın, Cevdet, Yesilyurt, Ahmet, Pınarlı, Ferda Alpaslan, Ersoy, Reyhan, Cakir, Bekir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618115/
https://www.ncbi.nlm.nih.gov/pubmed/26558116
http://dx.doi.org/10.1155/2015/296924

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618115/
https://www.ncbi.nlm.nih.gov/pubmed/26558116
http://dx.doi.org/10.1155/2015/296924

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