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Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees.

机译:对五个常染色体显性不躁腿综合征谱系的外显力和预期进行研究。

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摘要

Restless legs syndrome (RLS) can occur with an autosomal-dominant mode of inheritance. To determine if there are distinguishing features of RLS pedigrees which might clarify molecular mechanisms of pathogenesis, five pedigrees with 81 affected members were analyzed for age of onset, sex ratio, and transmission pattern. One-factor analysis of variance of ages of onset between generations was carried out, and segregation ratios were calculated for each generation. These kindreds showed an autosomal-dominant mode of inheritance and a male:female ratio of 1:1.4 (p = 0.15). One of the five analyzed pedigrees shows some evidence of reduced penetrance. In two of the five analyzed pedigrees, there is statistical support for anticipation (p<0.05). These variations in penetrance and anticipation suggest possible genetic heterogeneity.
机译:不正常的腿综合症(RLS)可能以常染色体显性遗传方式发生。为了确定RLS谱系是否具有明显的特征可以阐明发病机理,我们分析了81个受影响成员的5个谱系的发病年龄,性别比和传播方式。进行了几代之间发病年龄差异的单因素分析,并计算了每一代的分离率。这些亲戚显示出常染色体显性遗传模式,男女之比为1:1.4(p = 0.15)。五个被分析的家系之一显示出一些外表减少的证据。在五个分析的家谱中,有两个对预期有统计学支持(p <0.05)。外表和预期的这些变化表明可能存在遗传异质性。

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