Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy

Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy

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Non-classic congenital adrenal hyperplasia (NCAH) due to 21-hydroxylase deficiency is one of the actual causes of hyperandrogenic manifestations at different age intervals. Timely diagnosis of the disease requires evaluating basal 17-hydroxyprogesterone levels during the comprehensive examination of...

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Detalhes bibliográficos
Autor principal:	O.V. Rykova
Formato:	Artigo
Idioma:	English
Publicado em:	Zaslavsky O.Yu. 2019-09-01
Colecção:	Mìžnarodnij Endokrinologìčnij Žurnal
Assuntos:	congenital adrenal hyperplasia 21-hydroxylase hyperandrogenism polycystic ovary syndrome 17-hydroxyprogesterone
Acesso em linha:	http://iej.zaslavsky.com.ua/article/view/185410

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