中国男科学杂志
中國男科學雜誌
중국남과학잡지
CHINESE JOURNAL OF ANDROLOGY
2014年
5期
24-28,33
,共6页
陈美佳%吕福通%黄霈%华荣
陳美佳%呂福通%黃霈%華榮
진미가%려복통%황패%화영
少精子症%弱精子症%无精子症%死精子症%染色体畸变
少精子癥%弱精子癥%無精子癥%死精子癥%染色體畸變
소정자증%약정자증%무정자증%사정자증%염색체기변
oligospermia%asthenozoospermia%azoospermia%necrospermia%dysspermia%chromosome aberrations
目的:对少弱精子症、无精子症及死精子症的男性不育患者进行染色体分析,探讨染色体与生精异常之间的关系,及造成男性不育的机制。方法对328例少弱精子症、无精子症与死精子症的男性不育患者进行外周血淋巴细胞培养,常规G显带,计算机软件进行核型分析,计数30个核型,观察5个核型,异常者加倍分析。结果在328例生精异常男性不育患者中,发现染色体异常核型132例,异常检出率为40.2%,其中性染色体异常75例,占异常核型的56.8%;常染色体结构异常17例,占异常核型的12.9%;染色体多态现象40例,占异常核型的30.3%。经专家鉴定,有4例异常核型为国内外首次报道。结论染色体异常是引起男性生精异常的重要原因之一,在进行少弱精子症、无精子症或死精子症的临床诊断时,遗传因素不可忽视,这为确定是否有治疗价值提供重要依据。首报异常核型与临床资料的分析,为进一步研究男性生精异常及不育提供依据。
目的:對少弱精子癥、無精子癥及死精子癥的男性不育患者進行染色體分析,探討染色體與生精異常之間的關繫,及造成男性不育的機製。方法對328例少弱精子癥、無精子癥與死精子癥的男性不育患者進行外週血淋巴細胞培養,常規G顯帶,計算機軟件進行覈型分析,計數30箇覈型,觀察5箇覈型,異常者加倍分析。結果在328例生精異常男性不育患者中,髮現染色體異常覈型132例,異常檢齣率為40.2%,其中性染色體異常75例,佔異常覈型的56.8%;常染色體結構異常17例,佔異常覈型的12.9%;染色體多態現象40例,佔異常覈型的30.3%。經專傢鑒定,有4例異常覈型為國內外首次報道。結論染色體異常是引起男性生精異常的重要原因之一,在進行少弱精子癥、無精子癥或死精子癥的臨床診斷時,遺傳因素不可忽視,這為確定是否有治療價值提供重要依據。首報異常覈型與臨床資料的分析,為進一步研究男性生精異常及不育提供依據。
목적:대소약정자증、무정자증급사정자증적남성불육환자진행염색체분석,탐토염색체여생정이상지간적관계,급조성남성불육적궤제。방법대328례소약정자증、무정자증여사정자증적남성불육환자진행외주혈림파세포배양,상규G현대,계산궤연건진행핵형분석,계수30개핵형,관찰5개핵형,이상자가배분석。결과재328례생정이상남성불육환자중,발현염색체이상핵형132례,이상검출솔위40.2%,기중성염색체이상75례,점이상핵형적56.8%;상염색체결구이상17례,점이상핵형적12.9%;염색체다태현상40례,점이상핵형적30.3%。경전가감정,유4례이상핵형위국내외수차보도。결론염색체이상시인기남성생정이상적중요원인지일,재진행소약정자증、무정자증혹사정자증적림상진단시,유전인소불가홀시,저위학정시부유치료개치제공중요의거。수보이상핵형여림상자료적분석,위진일보연구남성생정이상급불육제공의거。
Objective To investigate the relationship between chromosome karyotype and male infertility of oligoasthenospermia, azoospermia, necrozoospermia, and explore the cause of male infertility. Methods Lymphocytes in peripheral blood from 328 male infertility with oligoasthenospermia, azoospermia or necrozoospermia were collected and cultured routinely and their chromosomes were stained by G banding.the karyotypes were analyzed by computer software. Results In the 328 cases of male infertility with dysspermia, 132 patients of them (40.2%) had abnormal karyotypeincluding 75sex chromosomal abnormality(56.8%), 17 autosomal structure abnormalities(12.9%), and 40 chromosomal polymorphism(30.3%). 4 rare karyotypes were first reported. Conclusion Chromosome abnormality was one of the important factors for male with dysspermia, so it is very essential to perform the genetic analysis for clinical diagnosis of oligoasthenospermia, azoospermia and necrozoospermia, as well as determining treatment methods. First reported karyotypes and clinical data provide the basis for better understanding dysspermia and male infertility.