基础医学与临床 ›› 2006, Vol. 26 ›› Issue (12): 1332-1334.

• 研究论文 • 上一篇    下一篇

男性平育患者的细胞遗传学分析

阿周存 林立   

  1. 云南大理学院生命科学与化学学院遗传学教研室 四川大学华西医院医学遗传室
  • 收稿日期:2006-02-14 修回日期:2006-06-30 出版日期:2006-12-25 发布日期:2006-12-25
  • 通讯作者: 阿周存

Cytogenetic analysis of male infertile patnts

  

  • Received:2006-02-14 Revised:2006-06-30 Online:2006-12-25 Published:2006-12-25

摘要: 目的 研究中国人群男性不育患者的染色体异常频率分布。方法 运用染色体G显带方法,对415例原发无精症或严重寡精症患者的核型进行分析。 结果 发现44例患者有染色体异常,频率为10.6%。结论 染色体异常是男性不育的一个常见遗传病因,在男性不育的诊断和卵细胞浆内单精子注射受精治疗前,对染色体的异常进行筛查十分必要。

Abstract: Objective To investigate the frequency of chromosome abnormality in male infertility in Chinese. Methods Karyotypes were analyzed by chromosome G-banding in 415 infertile patients with idiopathic azoospermia or severe oligozoospermia. Results 44(10.6%) of subjects were found to have chromosome abnormality. Conclusion The results of present study indicated that chromosome abnormality is one of the frequent genetic causes for male infertility, suggesting that it is essential to screen chromosome abnormality during diagnosis of male infertility as well as before in vitro assisted fertilization by intracytoplamic injection.