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Nonclassic Congenital Adrenal Hyperplasia

Nonclassic congenital adrenal hyperplasia (NCAH) due to P450c21 (21-hydroxylase deficiency) is a common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 gene which is located at chromosome 6p21. The clinical features predominantly reflect androgen excess rather than adr...

Полное описание

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Библиографические подробности
Главные авторы: Witchel, Selma Feldman, Azziz, Ricardo
Формат: Artigo
Язык:Inglês
Опубликовано: Hindawi Publishing Corporation 2010
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2910408/
https://ncbi.nlm.nih.gov/pubmed/20671993
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/625105
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