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[威廉姆斯-贝伦综合征及孤立性主动脉瓣上狭窄的遗传学研究。对128个家庭的调查(作者译)]

[The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)].

作者信息

Grimm T, Wesselhoeft H

出版信息

Z Kardiol. 1980 Mar;69(3):168-72.

PMID:7456592
Abstract

Supravalvular aortic stenosis (SVAS) was seen in 128 families. In 23 families several members had SVAS. In 4 families the Williams-Beuren Syndrome (WBS) was present whereas members of 8 families had some features of the syndrome in addition to their cardiac lesion. In conclusion, no distinct separation can be made between WBS and SVAS. The genetic pattern is autosomal dominant with variable expressivity. The gene frequency is estimated at 10(-4) and the mutation rate at 2.5 . 10(-5).

摘要

128个家族中发现有瓣上主动脉狭窄(SVAS)。在23个家族中,有几名成员患有SVAS。在4个家族中存在威廉姆斯-贝伦综合征(WBS),而8个家族的成员除了有心脏病变外,还具有该综合征的一些特征。总之,无法在WBS和SVAS之间做出明确区分。遗传模式为常染色体显性遗传,具有可变表达性。基因频率估计为10(-4),突变率为2.5×10(-5)。

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