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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Hlavní autor: O.V. Rykova
Médium: Článek
Jazyk:English
Vydáno: Zaslavsky O.Yu. 2019-09-01
Edice:Mìžnarodnij Endokrinologìčnij Žurnal
Témata:
congenital adrenal hyperplasia
21-hydroxylase
hyperandrogenism
polycystic ovary syndrome
17-hydroxyprogesterone
On-line přístup:http://iej.zaslavsky.com.ua/article/view/185410

Internet

http://iej.zaslavsky.com.ua/article/view/185410

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