Congenital adrenal hyperplasia: Treatment and outcomes

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. Glucocorticoid and mineralocorticoid replacement the...

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Bibliographic Details
Main Authors: Kamoun, Mahdi, Feki, Mouna Mnif, Sfar, Mohamed Habib, Abid, Mohamed
Format: Artigo
Language:Inglês
Published: Medknow Publications & Media Pvt Ltd 2013
Subjects:
Review Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3830282/
https://ncbi.nlm.nih.gov/pubmed/24251136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.119491
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