Management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children and adolescents: review

OBJECTIVE: To describe the diagnosis and clinical management of 21-hydroxylase deficiency (21OH-D), in the current context of including the disease in neonatal screening programs, as well as genetic, pathophysiological characteristics, and manifestations in childhood and adolescence. DATA SOURCE: I...

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Bibliographic Details

Published in:	Revista Médica de Minas Gerais
Main Authors:	Barra, Cristina Botelho, Silva, Ivani Novato
Format:	Article
Language:	English
Published:	Associação Médica de Minas Gerais 2022-08-01
Subjects:	congenital adrenal hyperplasia neonatal screening 21-hydroxylase deficiency glucocorticoid nr3c1 gene polymorphisms
Online Access:	http://www.rmmg.org/artigo/detalhes/3926