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特发性脊柱侧凸的分离分析:主要基因效应的证明

Segregation analysis of idiopathic scoliosis: demonstration of a major gene effect.

作者信息

Axenovich T I, Zaidman A M, Zorkoltseva I V, Tregubova I L, Borodin P M

机构信息

Department of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Russian Academy of Science, Novosibirsk, Russia.

出版信息

Am J Med Genet. 1999 Oct 8;86(4):389-94.

Abstract

Segregation analysis using a model with age and gender effects was applied to 101 pedigrees ascertained through a proband with idiopathic scoliosis. The transmission probability model was used to detect major gene effect. When we analyzed the pedigrees where affected status was assigned to persons with a Cobb's angle of more than 5 degrees we did not detect a significant major gene effect. However, when the affected status was assigned to persons with pronounced forms of disease only (a curve of at least 11 degrees) a significant contribution of a major causal gene could be established and inheritance could be described according to a dominant major gene diallele model, assuming incomplete sex and age dependent penetrance of genotypes. According to this model, the pronounced forms of idiopathic scoliosis should never occur in the absence of the mutant allele. This indicates that only the carriers of the mutant allele develop pronounced forms of the disease. At the same time, only a fraction of the carriers of the mutant gene should manifest the disease (30% of males and 50% of females).

摘要

使用具有年龄和性别效应的模型对通过特发性脊柱侧凸先证者确定的101个家系进行分离分析。采用传递概率模型检测主基因效应。当我们分析将Cobb角大于5度的人判定为患病状态的家系时,未检测到显著的主基因效应。然而,当仅将疾病的明显形式(至少11度的曲线)的人判定为患病状态时,可以确定一个主要致病基因的显著贡献,并且可以根据显性主基因双等位基因模型描述遗传方式,假设基因型存在不完全的性别和年龄依赖性外显率。根据该模型,在没有突变等位基因的情况下,特发性脊柱侧凸的明显形式永远不会出现。这表明只有突变等位基因的携带者会发展为疾病的明显形式。同时,只有一小部分突变基因的携带者会表现出疾病(30%的男性和50%的女性)。

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