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. 2006 Mar-Apr;52(2):87-90.
doi: 10.1080/01485010500315545.

Chromosomal abnormalities in patients with azoospermia in Western Mexico

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Chromosomal abnormalities in patients with azoospermia in Western Mexico

J P Meza-Espinoza et al. Arch Androl. 2006 Mar-Apr.

Abstract

In order to assess the frequency of chromosomal abnormalities in azoospermic males from western Mexico, we carried out a retrospective study in 227 patients. Forty-three (18.9%) cases with an abnormal karyotype were found. The most frequent chromosomal anomaly was 47,XXY, which was identified in 35 subjects (15.4%). In six cases (2.6%), structural aberrations were detected: two Robertsonian translocations [(45,XY,t(13;22)(p11;p11) and (45,XY,t(13;15)(p11;p11)], a Y;autosome translocation [46,XY,der(15)t(Y;15)(q12;p11)], and three mosaics [mos45,X/46,X,idic(Y)(q11)]. In general, these findings are in accordance with those from other surveys and confirm that the XXY aneuploidy is the most frequent chromosomal abnormality in azoospermic individuals.

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