期刊文献+

218例染色体异常者的细胞遗传学分析

Cytogenetical analysis on 218 cases with chromosomal abnormality
原文传递
导出
摘要 目的:对贵州省218例染色体异常者进行细胞遗传学分析,了解染色体异常情况,指导优生优育,提高出生人口素质。方法:对受检者常规询问病史、体格检查,抽取静脉血1.5ml进行淋巴细胞培养,中期染色体制片、G显带处理,每例患者镜下分别计数30个核型,分析核型3个以上,对异常者加大记数和分析量,并按人类细胞遗传学国际命名体制(ISCN,1985)的标准命名。结果:218例异常核型中常染色体数目、结构异常者150例(占68.8%),性染色体数目、结构异常者50例(占22.94%),染色体多态性18例(占8.26%)。结论:染色体异常与不良孕产史、不孕不育、智力低下、性发育异常、原发性闭经等有密切关系。进行孕前优生遗传咨询,及时了解染色体异常情况,对临床治疗及优生具有极其重要的指导意义。 Objective: To carry out cytogenetical analysis on 218 cases with chromosomal abnormality, understand the status of chromosomal abnormality in Guizhou, direct bearing and rearing better children and improve the quality of newborn babies. Methods: All the patients received history - taking and physical examination, then the cytogenetical analysis was carried out, the sequence was cultivation of lymphocytes from 1.5 milliliters venous blood, staining smear examination of metaphase chromosome, G binding and karyotype analysis. Results: Chromosomal abnormalities included: 150 cases of autosomal number and structural abnormality (68. 8% ), 50 cases of heterosomal number and structural abnormality (22. 94% ), 18 cases of chromosomal polymorphism ( 8.26% ) . Conclusion: Chromosomal abnormality is related to the history of adverse pregnancy, sterility and dysgenesis, feeblemindedness, abnormality of sexual development and primary amenorrhea. Genetic counseling of pregestational prepotency and understanding the status of chromosomal abnormality are important to clinical treatment and direct bearing and rearing better children.
出处 《中国妇幼保健》 CAS 北大核心 2009年第25期3537-3539,共3页 Maternal and Child Health Care of China
关键词 细胞遗传学 染色体 遗传咨询 Cytogenetics Chromosome Genetic counseling
  • 相关文献

参考文献4

二级参考文献14

  • 1张月萍 吕菊香 等.罗伯逊易位与自然流产[J].上海医科大学学报,1997,24:38-39.
  • 2辜土杨 施克珠 马堪悦 等.一例三代遗传性9号CS臂间倒位[J].天津医药,1988,8:468-468.
  • 3Jerome M F. Natural history of recurrent molar pregnancy. Obstet Gynecol, 1980, 55(4) :457
  • 4Buckley J D.The epidemiology of molar pregnancy and choriocarcinoma. Clin Obstet Gynecol, 1984,27(1): 153
  • 5何小轩 夏家辉 李麓芸 等.一例带有两条9号CS次缢痕丢失的患者及其家系的细胞遗传学研究[J].遗传学报,1982,9(4):315-315.
  • 6Reijo R, Lee TY, Salo P, et al. Diverse spermatogenic effects in humans caused by Y chromosome deletions encompassing a novel RNA - binding protein gene. Nature Genet, 1995,10:383
  • 7Na jmabadi, Huang V, Yen P, et al. Substantial prevalence of microdeletions of Y chromosome in infertile men with idiopathic azoospermia and oligosperia detected using a seguence - tagged site- based mapping stretegy. J Clin Endocrinol Metab, 1996,81:1347
  • 8Ma K, Inglis JD, Sharkey A, et al. A Y chromosome gene family with RNA- binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis. Cell, 1993,73: 1287.
  • 9Jones C, Am J.The relation between the variation of double nucleoar zone and Turner's syndrome. Med. genet, 1988,30: 725 - 732
  • 10李鸿雁,连小华,刘伟.染色体异态性与染色体不分离关系的初步探讨[J].中国优生与遗传杂志,1998,6(4):32-32. 被引量:1

共引文献66

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部