染色体端到端融合在完全性共济失调(AT)中的串联重复q14和双中心形成。5例患者的临床及细胞遗传学表现。

Humangenetik Pub Date : 1975-11-06 DOI:10.1007/BF00291946
K Hayashi, W Schmid
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引用次数: 60

摘要

对5例AT患者进行淋巴细胞培养染色体研究,其中2例随访4年。这些患者中有4人显示出染色体型畸变的发生率增加。一名患者出现克隆发育,96%的中期包含几乎整个长臂14的串联重复。四年前,这些细胞的比例是80%。另外两名患者表现出一小部分细胞具有未知的异常长D染色体。在4例患者的724个中期中,观察到31条双中心染色体,均为一种特殊类型;在它们的形成过程中,没有染色体物质丢失,它们似乎都是端到端融合产生的。5例患者的染色单体型畸变发生率均正常或处于控制值的上限。用BUDR检测3例患者的姊妹染色单体交换率均正常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telandiectasia (AT). Clinical and cytogenetic findings in 5 patients.

Chromosome studies on lymphocyte cultures were performed in 5 patients with AT, 2 of whom had been followed for 4 years. Four out of these patients showed an increased incidence of chromosome-type aberrations. A clonal development was present in one patient, 96% of his metaphases containing a tandem duplication of almost the entire long arm 14. Four years earlier the proportion of these cells was 80%. Two other patients presented a small proportion of cells with an unidentified abnormally long D chromosome. In a total of 724 metaphases from 4 patients 31 dicentric chromosomes were observed, all of a peculiar type; in their formation no chromosome material was lost and they all seem to have arisen by end-to-end fusions. The incidence of chromatid-type aberrations was normal or at the upper limit of control values in all 5 cases. The sister chromatid exchange rate studied with BUDR in 3 patients was found to be normal.

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