Objectives
To detect autosomal genetic defects and to determine candidate genes in Sertoli cell‐only syndrome infertile men.
Methods
Single‐nucleotide polymorphism + comparative genomic hybridization microarray technology was carried out on 39 Sertoli cell‐only syndrome infertile patients in the present study. Array comparative genomic hybridization compares the patient's genome against a reference genome, and identifies uncover deletions, amplifications and loss of heterozygosity.
Results
A link between defective spermatogenesis genes and infertility was examined, and amplifications and deletions in several genes were detected, including homeobox gene; synaptonemal complex element protein 1; collagen, type I, alpha 1; imprinted maternally expressed transcript; and potassium voltage‐gated channel subfamily Q member 1.
Conclusions
The present data suggest that several genes can play an important role in spermatogenesis and progression of Sertoli cell‐only syndrome.
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