A study of Y-chromosome microdeletions in the male infertility
Wei Hui-pin
Abstract
Wei Hui-pin
Abstract
Objective: To study associations with azoospermia and oligozoospermia and Y chromosome microdeletions.To establish a method for molecular diagnosis of Y chromosome microdeletions.Methods: Multiplex PCR amplification of 6 STS in AZF regions of the Y chromosome was examined among 53 examples normal karyotype male patients with azoospermia and oligozoospermia and 5 examples normal men.Results: No Y chromosome microdeletions were found among 5 normal men.6 cases exist microdeletions in AZF region among 53 male patients.The microdeletions rate is 11.3%.Conclusion: Microdeletions of Y chromosome is one of the major causes of severe dyszoospermia;the gene of AZF may be plays an important role in the course of spermatogentics.
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Objective: To study associations with azoospermia and oligozoospermia and Y chromosome microdeletions.To establish a method for molecular diagnosis of Y chromosome microdeletions.Methods: Multiplex PCR amplification of 6 STS in AZF regions of the Y chromosome was examined among 53 examples normal karyotype male patients with azoospermia and oligozoospermia and 5 examples normal men.Results: No Y chromosome microdeletions were found among 5 normal men.6 cases exist microdeletions in AZF region among 53 male patients.The microdeletions rate is 11.3%.Conclusion: Microdeletions of Y chromosome is one of the major causes of severe dyszoospermia;the gene of AZF may be plays an important role in the course of spermatogentics.
Key concepts: Y chromosome microdeletion, Azoospermia factor, Y chromosome, Azoospermia, Male infertility, Karyotype, Chromosome, Gynecology