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132例男性不育患者遗传学病因分析
引用本文:宋丹,钱卫平,许晓清,谭玉梅.132例男性不育患者遗传学病因分析[J].临床泌尿外科杂志,2004,19(9):543-544.
作者姓名:宋丹  钱卫平  许晓清  谭玉梅
作者单位:深圳市罗湖医院生殖中心,广东,深圳,518001
摘    要:目的:对男性不育患者进行遗传学病因分析,并探讨其遗传效应。方法:采取132例男性不育患者外周血进行染色体核型分析。结果:132例男性不育患者中,染色体异常24例,染色体变异22例。其中大Y20例,47,XXY18例,45.XY,t(13;14)3例,小Y和46,XY,inv(9)各2例,46,XY,t(9;22)1例。结论:染色体异常是男性不育的重要原因,并建议男性不育患者进行基因诊断,以便确诊是否属于遗传病,为生育提供指导,避免盲目治疗。

关 键 词:男性不育  染色体异常  遗传效应
文章编号:1001-1420(2004)09-0543-02
修稿时间:2004年5月13日

Genetic analysis of 132 infertile men
SONG Dan,QIAN Weiping,XU Xiaoqing,TAN Yumei.Genetic analysis of 132 infertile men[J].Journal of Clinical Urology,2004,19(9):543-544.
Authors:SONG Dan  QIAN Weiping  XU Xiaoqing  TAN Yumei
Institution:SONG Dan 1 QIAN Weiping 1 XU Xiaoqing 1 TAN Yumei 1
Abstract:Objective:To study the genetic effect on man infertility according to their karotypes.Method:Karyotypes of 132 infertile men were analyzed by chromosome G banding and C banding methods.Results:24 various abnormal karyotypes and 22 chromosome polymorphisms were found in 132 cases, including 20 case of Yqh+, 18 cases of Klinefelter's syndrome, 3 cases of 45, XY, t(13;14); 2 cases of Yqh- and 46, XY, inv(9) each, 1 case of 46, XY, t(9;22).Conclusions:Chromosomal abnormality is an important cause in male infertility. Gene diagnosis was advised to diagnose genetic disease or not, which offer guidance on reproduction and avoid blindness therapy.
Keywords:Male infertility  Chromosome abnormality  Genetic effect
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