Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Congenital adrenal hyperplasia (CAH) describes a group of autosomal recessive disorders where there is impairment of cortisol biosynthesis. CAH due to 21-hydroxylase deficiency accounts for 95% of cases and shows a wide range of clinical severity. Treatment of the classic or severe form of CAH is ta...

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Bibliographic Details
Main Author: Merke, Deborah P.
Format: Artigo
Language:Inglês
Published: The Endocrine Society 2008
Subjects:
Approach to the Patient
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2266964/
https://ncbi.nlm.nih.gov/pubmed/18326005
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2007-2417
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