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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Detalles Bibliográficos
Autores principales: Falhammar, Henrik, Farber, Robert, Chan, Jean L, Farrar, Mallory, Yonan, Chuck, Kuranz, Seth, Auchus, Richard J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208752/
http://dx.doi.org/10.1210/jendso/bvaa046.374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208752/
http://dx.doi.org/10.1210/jendso/bvaa046.374

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