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1564例脐血细胞染色体核型分析 [中文引用][英文引用]

1564 Cases of Chromosomal Karyotype Analysis of Fetal Cord Blood

作者(英文):Wang Dan  Wang Hua  Huang Ding-mei  Jia Zheng-jun  Peng Xiang-jun  Zhou Yu-chun 
单位(英文):Maternal and Child Health Hospital of Hunan Province 
关键词:脐带穿刺 染色体异常 
关键词(英文):cordocentesis  prenatal diagnosis  chromosomal karyotypes 
分类号:R714.7
出版年·卷·期(页码):2011·3·第4期(18-21)
DOI: 20110405
-----摘要:-------------------------------------------------------------------------------------------

目的 探讨脐带穿刺在产前诊断中的作用了解染色体异常核型与产前诊断指征的关系为遗传咨询与产前诊断提供依据方法 20016月至20116月在湖南省妇幼保健院就诊的1564例染色体病高危孕妇进行脐带穿刺取脐血细胞培养制备中期染色体常规G显带分析胎儿核型进行产前诊断结果 1564例产前诊断对象中检出胎儿染色体异常核型90检出率5.8%数目异常为主要的染色体异常以三体型为主49.6%其中21三体占45.8%结论 在高危孕妇中进行脐血穿刺是产前诊断的重要方法同时结合孕母血清筛查B超检查及高龄等是发现染色体病胎儿预防出生缺陷的重要措施

-----英文摘要:---------------------------------------------------------------------------------------

Objective  To analyze the value of chromosomal karyotypes of fetal cordblood for prenatal diagnosis, and to investigate the relationship between the chromosomal abnormalities and the indications of prenatal diagnosis, providing the basis for hereditary consultation and prenatal diagnosis. Methods  Cordocentesis were performed in 1564 pregnant women diagnosis during the June 2001 to Jun e2011, and fetal chromosomal karyotypes were examined. Results  90 chromosomal abnormalities(5.8%) were checked out. Trisomy, the leading abnormality, consisted of 49.6% of all abnormalities and trisomy 21, which was 45.8%. Conclusion  Cordblood for prenatal diagnosis of chromosomal diseases is important; and it is the major step of the diagnostic rate of chromosomal abnormalities and preventing birth defect with the prenatal serum screening, antenatal ultrasound screening and advanced age can increase.

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若需在您的论文中引用此文,请按以下格式著录参考文献:
中文著录格式: 王丹,王华,黄定梅,贾政军,彭向京,周玉春.1564例脐血细胞染色体核型分析.中国产前诊断杂志,2011,3(4):18-21.
英文著录格式: Wang,Dan,,Wang,Hua,,Huang,Ding-mei,,Jia,Zheng-jun,,Peng,Xiang-jun,,Zhou,Yu-chun.1564 Cases of Chromosomal Karyotype Analysis of Fetal Cord Blood.No Title Settings,2011,3(4):18-21.

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