少弱精子症、死精子症、无精子症患者细胞遗传学分析  

Analysis of chromosome karyotypes for patients with oligoasthenospermia,azoospermia and necrozoospermia

作　　者：孔舒[1] 孙筱放[1] 郑育红[1] 黎青[1] 

机构地区：[1]广州医学院第三附属医院妇产科研究所实验部,广州市生殖与遗传实验部,广州510150

出　　处：《中国优生与遗传杂志》2012年第7期51-52,共2页Chinese Journal of Birth Health & Heredity

摘　　要：目的了解少弱精子症、死精子症、无精子症与染色体之间的联系。方法对2011年上半年生殖门诊101例少弱精子症、死精子症、无精子症患者,进行染色体检测,并对结果进行比较分析。结果染色体异常总数占23例,异常发生率达22.8%。性染色体异常9例,占异常总数的39%,常染色体异常14例,占异常总数61%。结论男性不育少弱精子症、死精子症、无精子症患者常规做染色体检查是必要的,对确定其是否有治疗价值提供重要依据。Objectives： To investigate on the relationship between occurrence of oligoasthenospermia, azoospermia, necrozoospermia and parameters of chromosome. Methods： To detect the chromosome for the 101 patients with oligoasthenospermia, azoospermia and necrozoospermia in the first half of 2011. Results： The total number of abnormal chromosomes is 23 cases （22. 8% ）. The number of abnormal sex chromosomes is 9 cases, accounting for 39% of the total abnormal chromosomes, while the number of abnormal euchromosomes is 14, accounting for 62%. Conclusion： It is necessary for oligoasthenospermia, azoospermia and necrozoospermia patients to take routine chromosome and semen hormone tests. This will provide important reference for treatment.

关 键 词：少弱精子症 死精子症 无精子症 染色体 

分 类 号：R698.2[医药卫生—泌尿科学]