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未培养羊水荧光原位杂交快速检测60例胎儿常见染色体数目异常
引用本文:王昊,李海波,王辉林,王华,夏艳,文娟,龙志高,戴和半,梁德生,夏家辉,邬玲仟.未培养羊水荧光原位杂交快速检测60例胎儿常见染色体数目异常[J].中华医学遗传学杂志,2008,25(5):538-541.
作者姓名:王昊  李海波  王辉林  王华  夏艳  文娟  龙志高  戴和半  梁德生  夏家辉  邬玲仟
作者单位:1. 410078,长沙,中南大学中国医学遗传学国家重点实验室;湘雅医院产前诊断中心
2. 湖南省妇幼保健院
基金项目:国家自然科学基金,国家科技支撑项目 
摘    要:目的 应用细菌人工染色体(bacterial artificial chromosome,BAC)克隆自行制备荧光探针,对胎儿常见染色体数目异常(13,18,21,X,Y)行快速产前诊断.方法 利用中国医学遗传学国家重点实验室BAC库中相应染色体特异位点克隆,自行制备荧光探针.经外周血淋巴细胞染色体杂交验证后,用于胎儿未培养羊水的快速荧光原位杂交fluorescence in situ hybridization,FISH)检测,已检测60例羊水标本.结果 所有探针特异性均为100%,杂交成功率为97.86%;FISH结果与常规核型分析一致,检出21三体2例,18三体1例.有两例涉及其它染色体的结构异常未能检出.结论 自制探针用于未培养羊水快速FISH,使用标本量少、快速、简便,可有效检出上述5种染色体的数目异常,但本法不能检出其他染色体的数目异常和结构异常,其应用仍有一定局限性.

关 键 词:间期荧光原位杂交  未培养羊水  产前诊断  非整倍体

Rapid prenatal diagnosis of chromosome aneuploidies in60 uncultured amniotic fluid samples by fluorescence in situ hybridization
WANG Hao,LI Hai-bo,WANG Hui-lin,WANG Hua,XIA Yan,WEN Juan,LONG Zhi-gao,DAI He-ping,LIANG De-sheng,XIA Jia-hui,WU Ling-qian.Rapid prenatal diagnosis of chromosome aneuploidies in60 uncultured amniotic fluid samples by fluorescence in situ hybridization[J].Chinese Journal of Medical Genetics,2008,25(5):538-541.
Authors:WANG Hao  LI Hai-bo  WANG Hui-lin  WANG Hua  XIA Yan  WEN Juan  LONG Zhi-gao  DAI He-ping  LIANG De-sheng  XIA Jia-hui  WU Ling-qian
Institution:State Key Lab of Medical Genetics of China, Central South University, Changsha, Hunan 410078, P.R. China.
Abstract:OBJECTIVE: To evaluate the feasibility of rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization (FISH) using uncultured amniotic fluid. METHODS: Bacterial artificial chromosome (BAC) DNA probes were prepared and validated by using cultured peripheral blood. Interphase FISH for chromosomes 13, 18, 21, X and Y was performed in 60 amniotic fluid samples for the rapid prenatal diagnosis of chromosome aneuploidies, and the results were compared with the karyotypes from conventional cytogenetic analysis. RESULTS: Of all 60 cases, 58 were concordant with their karyotypes, and 1 case of inv(9) and another case of t(2,12) were identified by karyotyping. Two cases of trisomy 21 and 1 case of trisomy 18 were detected by FISH and confirmed with conventional cytogenetics (sensitivity=100%). There were no false-positive or false-negative results. CONCLUSION: This evaluation demonstrated that FISH employing BAC DNA probes could accurately and rapidly detect aneuploidies involving the above 5 chromosomes. However, as it does not identify structural chromosome aberrations and aneuploidies involving other chromosomes, it is not a substitute for conventional chromosome analysis, and the negative FISH result should be carefully interpreted.
Keywords:fluorescence in situ hybridization  uncultured amniotic fluid  prenatal diagnosis  aneuploidy
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