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Relationship of genetic causes and inhibin B in non obstructive azoospermia spermatogenic failure

Authors :
Qing-jun Chu
Rui Hua
Chen Luo
Qing-jie Chen
Biao Wu
Song Quan
Yong-tong Zhu
Source :
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
Publication Year :
2017
Publisher :
BMC, 2017.

Abstract

Abstract Background Chromosomal disorders in non obstructive azoospermia (NOA) may have an important influence on spermatogenesis, which may be reflected by the serum inhibin B levels. Till now, few studies have concerned the relationship of genetic causes and inhibin B in NOA. Methods In this retrospective study, 322 men with NOA in Center for Reproductive Medicine, Nanfang Hospital, Southern Medical University were collected. The level of follicle stimulating hormone (FSH), inhibin B, Y chromosome microdeletion test (YCMD) and karyotype were measured. Results Abnormal karyotypes were present in 38.5% of NOA, and YCMD were present in 18.0%, there was a high correlation between karyotypes and YCMD (χ2 = 11.892, P

Details

Language :
English
ISSN :
14712350
Volume :
18
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Medical Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.fcf27533e9774e179e29a3d13ec1afa9
Document Type :
article
Full Text :
https://doi.org/10.1186/s12881-017-0456-x