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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Bibliographic Details
Main Author: O.V. Rykova
Format: Article
Language:English
Published: Publishing House Zaslavsky 2019-08-01
Series:Mìžnarodnij Endokrinologìčnij Žurnal
Subjects:
congenital adrenal hyperplasia
21-hydroxylase
hyperandrogenism
polycystic ovary syndrome
17-hydroxyprogesterone
Online Access:http://iej.zaslavsky.com.ua/article/view/180044

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