MON-183 Adrenal Androgen Control and Steroidal Side Effects in Adolescents and Adults with Congenital Adrenal Hyperplasia Treated with Glucocorticoids

Introduction: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rare autosomal recessive disorder that results in little or no cortisol biosynthesis, increased production of precursor steroids, and excess production of adrenal androgens. Glucocorticoid (GC) treatment...

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Bibliografiske detaljer
Udgivet i:J Endocr Soc
Main Authors: Falhammar, Henrik, Farber, Robert, Chan, Jean L, Farrar, Mallory, Yonan, Chuck, Kuranz, Seth, Auchus, Richard J
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2020
Fag:
Adrenal
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208752/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.374
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