Congenital adrenal hyperplasia (21-hydroxylase deficiency) in adulthood patients: diagnosis and treatment

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Abstract

In the article presents the main approaches to the diagnosis and treatment of patients with classical and nonclassical forms 21-hydroxylase deficiency. The techniques of diagnostic tests and parameters of hormonal indicators to assess the adequacy of replacement therapy glucocorticoids and mineralocorticoids are considered.

About the authors

N. V Molashenko

Endocrinology Research Center of the Ministry of Health of the Russian Federation

Email: molashenko@mail.ru
канд. мед. наук, вед. науч. сотр. отд. терапевтической эндокринологии ФГБУ ЭНЦ 117036, Russian Federation, Moscow, ul. Dmitria Ul'ianova, d. 11

A. I Sazonova

V.I.Kulakov Research Center for Obstetrics, Gynecology and Perinatology of the Ministry of Health of the Russian Federation

канд. мед. наук, врач-эндокринолог терапевтического отд-ния ФГБУ «НЦАГиП им. акад. В.И.Кулакова» 117997, Russian Federation, Moscow, ul. Akademika Oparina, d. 4

E. A Troshina

Endocrinology Research Center of the Ministry of Health of the Russian Federation

акад. РАН, д-р мед. наук, проф., зав. отд. терапевтической эндокринологии ФГБУ ЭНЦ 117036, Russian Federation, Moscow, ul. Dmitria Ul'ianova, d. 11

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