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两例患有罕见新发易位的唐氏综合征病例。

Two cases of Down syndrome with unusual de novo translocation.

作者信息

Verma R S, Peakman D C, Robinson A, Lubs H A

出版信息

Clin Genet. 1977 Mar;11(3):227-34. doi: 10.1111/j.1399-0004.1977.tb01305.x.

Abstract

Two children with the clinical features of Down syndrome were found to have several unusual cell lines. In both cases the same reverse tandem translocation between two 21 chromosomes was present in one line. This may be an unstable rearrangement. In addition, the findings offer some support for current efforts to localize the portion of chromosome 21 responsible for clinical features of Down syndrome to band 21q22. Acridine orange R banding was found to be especially useful in the identification of the break points on the translocations. The origin of the abnormality was found to be paternal in one case and was indeterminate in the second.

摘要

发现两名具有唐氏综合征临床特征的儿童有几种异常细胞系。在这两个病例中,一条细胞系中两条21号染色体之间存在相同的反向串联易位。这可能是一种不稳定的重排。此外,这些发现为目前将21号染色体上与唐氏综合征临床特征相关的部分定位到21q22带的研究提供了一些支持。发现吖啶橙R显带在识别易位的断点方面特别有用。在一个病例中发现异常起源于父方,在另一个病例中则无法确定。

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