Clinical Features of Classical Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency with Complete Virilisation

Background: The most prevalent form of Congenital adrenal hyperplasia (CAH) is 21-hydroxylase deficiency (21-OHD), which accounts for over 90% of CAH cases. This enzymatic defect results in decreased cortisol and aldosterone synthesis, leading to compensatory adrenocorticotropic hormone (ACTH) secre...

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Bibliographic Details
Published inAsian Journal of Advanced Research and Reports Vol. 19; no. 8; pp. 317 - 322
Main Authors Anguoud, Houda El, Agarrab, Noura, Gaouzi, Ahmed, Imane, Zineb, Alaoui, Asmaa Mdaghri
Format Journal Article
LanguageEnglish
Published 20.08.2025
Subjects
Computer Science
Medical Imaging
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