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共济失调毛细血管扩张症遗传中的异常特征。

Unusual features in the inheritance of ataxia telangiectasia.

作者信息

Woods C G, Bundey S E, Taylor A M

机构信息

Sub Department of Clinical Genetics, University of Birmingham, Birmingham Maternity Hospital, Edgbaston, UK.

出版信息

Hum Genet. 1990 May;84(6):555-62. doi: 10.1007/BF00210809.

Abstract

A prevalence study of ataxia telangiectasia was conducted in the West Midlands, with a population of over 5 million. The prevalence in those aged 50 or less was found to be 1 in 514,000 and the birth frequency to be about 1 in 300,000. A genetic study of 47 families ascertained throughout the United Kingdom was carried out concurrently. A low parental consanguinity rate was found, no parents being first cousins or more closely related, whereas 10% had been expected. The incidence of ataxia telangiectasia in the 79 sibs of index cases was 1 in 7. These two features demonstrate that ataxia telangiectasia may not always be an autosomal recessive condition. Other possible explanations are that some cases are double heterozygotes or new dominant mutations.

摘要

在西米德兰兹郡进行了一项共济失调毛细血管扩张症的患病率研究,该地区人口超过500万。研究发现,50岁及以下人群中的患病率为1/514,000,出生频率约为1/300,000。同时,对全英国确定的47个家庭进行了基因研究。结果发现父母近亲结婚率较低,没有父母是一级表亲或血缘关系更近的,而预期该比例为10%。索引病例的79名同胞中,共济失调毛细血管扩张症的发病率为1/7。这两个特征表明,共济失调毛细血管扩张症可能并不总是常染色体隐性疾病。其他可能的解释是,一些病例是双重杂合子或新的显性突变。

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