孤立病例正常亲属受不完全渗透条件影响的杂合概率及其后代复发风险的计算。常染色体显性基因。

American Journal of Medical Genetics Pub Date : 2000-11-06
P A Otto, S R Maestrelli
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引用次数: 0

摘要

由不完全显性常染色体显性基因产生的孤立病例亲属的杂合度概率P(het)及其后代的复发风险,R = P(het)。K/2,其中K为外显率值,在一些简单的特殊情况下已经在文献中计算过。贝叶斯定理和有限差分方程理论中的元素使我们能够推导出任何属于包含不完全渗透常染色体显性遗传病孤立病例的家系的个体的杂合概率。这里导出的广义公式对迄今为止文献中研究过的大多数特殊情况都是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes.

Heterozygosity probabilities P(het) for relatives of isolated cases produced by incompletely penetrant autosomal dominant genes and recurrence risks for their offspring, R = P(het).K/2, where K is the penetrance value, have been calculated in the literature for some simple particular situations. Bayes theorem and elements from the theory of finite difference equations enabled us to derive the heterozygosity probability for any individual belonging to a pedigree containing an isolated case affected with an incompletely penetrant autosomal dominant disorder. The generalized formula here derived is valid for most particular cases thus far studied in the literature.

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