1.Prevalence of Y chromosome microdeletions among infertile Mongolian men
Erdenesuvd DAMDINSUREN ; Purevjargal NAIDANSUREN ; Mendsaikhan GOCHOO ; Bum-Chae CHOI ; Min-Youp CHOI ; Bolorchimeg BALDANDORJ
Clinical and Experimental Reproductive Medicine 2022;49(2):101-109
		                        		
		                        			 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. 
		                        		
		                        		
		                        		
		                        	
            
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