Prevalence of Y chromosome microdeletions among infertile Mongolian men

Author:

Damdinsuren ErdenesuvdORCID,Naidansuren PurevjargalORCID,Gochoo MendsaikhanORCID,Choi Bum-ChaeORCID,Choi Min-YoupORCID,Baldandorj BolorchimegORCID

Abstract

Objective: Y chromosome microdeletions are the second most common genetic cause of male infertility after Klinefelter syndrome. The aim of this study was to determine the patterns of Y chromosome microdeletions among infertile Mongolian men.Methods: A descriptive study was performed on 75 infertile men from February 2017 to December 2018. Y chromosome microdeletions were identified by polymerase chain reaction. Semen parameters, hormonal levels, and testis biopsy samples were examined.Results: Among 75 infertile men, two cases of Y chromosome microdeletions were identified. The first case had an AZFa complete deletion and the other had an AZFc partial deletion. This study found that the proportion of Y chromosome microdeletions among infertile Mongolian men was 2.66%.Conclusion: The findings can be applied to in vitro fertilization and assisted reproductive technology, and our results will help clinicians improve treatment management for infertile Mongolian couples.

Publisher

The Korean Society for Reproductive Medicine

Subject

Reproductive Medicine

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