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共济失调毛细血管扩张症的细胞遗传学研究

Cytogenetic study on ataxia telangiectasia

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【作者】 张影如陈嵘梁秀龄欧翠华

【Author】 Zhang Yingru,Chen Rong,Liang Xiuling,et al.Department of Neurology,First Affiliated Hospital,Sun Yat Sen University of Medical Sciences,Guangzhou 510080

【机构】 广州中山医科大学附属第一医院神经科

【摘要】 目的探讨共济失调毛细血管扩张症的细胞遗传学异常特点。方法收集来自3个家系本病患者6例,进行外周血淋巴细胞G显带分析。结果6例患者中4例有染色体异常,在该4例患者所分析的129个细胞中,43个细胞有核型异常,累及1、7、14、2、4、6、11、17号染色体的分别有18、18、15、3、2、1、1、1个细胞;43个异常核型细胞中,缺失、易位、染色体断裂、双着丝粒、倒位各有19、16、4、1、1个细胞。结论1号染色体与7号、14号染色体一样,均是本病最不稳定的染色体,缺失和易位是本病细胞遗传学最常见的异常方式

【Abstract】 Objective To investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.Methods The clinical data of 6 patients from 3 ataxia telangiectasia families were reported,and their peripheral blood lymphocyte chromosomes were studied by G banding analysis. Results Chromosome abnormalities were found in 43 cells among 129 analyzed lymphocytes from 4 patients,while 2 other patients without abnormal chromosomes.Chromosome 1,7,14,2,4,6, 11,17 abnormalities were found respectively in 18,18,15,3,2,1,1,1 cells.Among 43 cells with abnormal chromosomes,deletion,translocation,dicentrics,csb and inversion were demonstrated in 19,16,4,1 and 1 cells. Conclusions Chromosome 1 is the most unstable one in the disease like chromosome 7 and 14.Deletion and translocation are the most common abnormalities.

  • 【文献出处】 临床神经病学杂志 ,JOURNAL OF CLINICAL NEUROLOGY , 编辑部邮箱 ,1999年02期
  • 【被引频次】1
  • 【下载频次】75
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