| Literature DB >> 22731643 |
Myriam Ghorbel1, Siwar Baklouti Gargouri, Nacira Zribi, Fatma Ben Abdallah, Mariem Cherif, Rim Keskes, Nozha Chakroun, Afifa Sellami, Ken McElreavey, Faiza Fakhfakh, Leila Ammar-Keskes.
Abstract
Azoospermia factor (AZF) subdeletions were reported to be significant risk factors for spermatogenesis. In this study, we screened classical and partial microdeletions of the Y-chromosome AZF region in a group of 261 infertile men. Partial deletions were also screened in a control group of fertile men (n=124). In addition, Y haplogroups were analyzed in 24 gr/gr deleted patients. Among the 261 studied infertile men, seven subjects were found to have classical microdeletions. The most common partial deletion of AZFc (gr/gr) was observed in 13.02% of infertile men and in 12.90% of fertile men. The b1/b3 deletion was identified in 4.98% of infertile men and in 2.41% of fertile men. In addition, the b2/b3 deletion was identified in 1.53% of infertile patients but not in the control group. Our results suggest that partial AZFc deletions are not associated with spermatogenic failure in the Tunisian population.Entities:
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Year: 2012 PMID: 22731643 DOI: 10.1089/gtmb.2012.0024
Source DB: PubMed Journal: Genet Test Mol Biomarkers ISSN: 1945-0257