De novo chromosomal translocation t(3;5)(q13;q35) in an infertile man

被引：5
|
作者：
Venkateshwari, A. [1 ,2 ]
Srilekha, A. [1 ,2 ]
Begum, A. [1 ,2 ]
Sujatha, M. [1 ,2 ]
Sunitha, T. [1 ,2 ]
Nallari, P. [3 ]
Jyothy, A. [1 ,2 ]
机构：
[1] Osmania Univ, Inst Genet, Hyderabad 500016, Andhra Pradesh, India
[2] Osmania Univ, Hosp Genet Dis, Hyderabad 500016, Andhra Pradesh, India
[3] Osmania Univ, Dept Genet, Hyderabad 500016, Andhra Pradesh, India
来源：
ANDROLOGIA | 2011年 / 43卷 / 06期
关键词：
Chromosomal translocation; infertility; karyotype; oligozoospermia; repeated abortions; RECIPROCAL TRANSLOCATIONS; ANOMALIES;
D O I：
10.1111/j.1439-0272.2010.01069.x
中图分类号：
R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
摘要：
Chromosomal rearrangements are rare structural abnormalities that are usually associated with male infertility or sterility. We describe here the clinical and cytogenetic studies carried out in a couple with repeated abortions. Cytogenetic analysis of the male partner showed a de novo chromosomal translocation t(3;5)(q13;q35) which could be involved in the meiotic errors resulting in reproductive failure.
引用
收藏
页码：428 / 430
页数：3
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