Woods C G, Bundey S E, Taylor A M
Sub Department of Clinical Genetics, University of Birmingham, Birmingham Maternity Hospital, Edgbaston, UK.
Hum Genet. 1990 May;84(6):555-62. doi: 10.1007/BF00210809.
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.
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。