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Genetic markers of polycystic ovary syndrome: role in the pathogenesis and phenotypic manifestations of the disease

https://doi.org/10.33667/2078-5631-2022-24-44-47

Abstract

Polycystic ovary syndrome is currently regarded as a multifactorial disease with a genetic predisposition, characterized by a wide variability in clinical manifestations that affect the reproductive, endocrine and metabolic functions of women. Despite the great scientific interest in this pathology, the causes and mechanisms of development remain not fully understood. In this article, we reviewed the most current research on the genetic markers of PCOS.

About the Authors

A. B. Khuraseva
Kursk State Medical University
Russian Federation

Khuraseva Anna B., DM Sci (habil.), professor, Department of Obstetrics and Gynecology Institute of Continuing Education

Kursk



K. S. Svyatchenko
Zhivitsa Medical Center
Russian Federation

Svyatchenko Ksenia S., obstetrician-gynecologist

Kursk



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Review

For citations:


Khuraseva A.B., Svyatchenko K.S. Genetic markers of polycystic ovary syndrome: role in the pathogenesis and phenotypic manifestations of the disease. Medical alphabet. 2022;(24):44-47. (In Russ.) https://doi.org/10.33667/2078-5631-2022-24-44-47

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ISSN 2078-5631 (Print)
ISSN 2949-2807 (Online)