Literature DB >> 22731643

Partial microdeletions in the Y-chromosome AZFc region are not a significant risk factor for spermatogenic impairment in Tunisian infertile men.

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.

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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


  4 in total

1.  Susceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions.

Authors:  S Sen; P Ambulkar; I Hinduja; K Zaveri; J Gokral; A Pal; D Modi
Journal:  J Assist Reprod Genet       Date:  2015-07-07       Impact factor: 3.412

2.  Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses.

Authors:  Sandeep Kumar Bansal; Deepika Jaiswal; Nishi Gupta; Kiran Singh; Rima Dada; Satya Narayan Sankhwar; Gopal Gupta; Singh Rajender
Journal:  Sci Rep       Date:  2016-02-15       Impact factor: 4.379

3.  An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis.

Authors:  Shinnosuke Kuroda; Kimitsugu Usui; Kohei Mori; Kengo Yasuda; Takuo Asai; Hiroyuki Sanjo; Hiroyuki Yakanaka; Teppei Takeshima; Takashi Kawahara; Haruka Hamanoue; Yoshitake Kato; Yasuhide Miyoshi; Hiroji Uemura; Akira Iwasaki; Yasushi Yumura
Journal:  Clin Exp Reprod Med       Date:  2018-03-30

4.  Deletion of b1/b3 shows risk for expanse of Yq microdeletion in male offspring: Case report of novel Y chromosome variations.

Authors:  Xiangyin Liu; Hongguo Zhang; Yang Yu; Jia Fei; Yuting Jiang; Ruizhi Liu; Ruixue Wang; Guirong Zhang
Journal:  Medicine (Baltimore)       Date:  2020-09-11       Impact factor: 1.817

  4 in total

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