婴儿肥厚性幽门狭窄的遗传学。再分析。

L E Mitchell, N Risch
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引用次数: 120

摘要

目的:确定现有的婴儿肥厚性幽门狭窄(IHPS)家族资料是否足以建立该疾病的遗传模式。设计:重新分析IHPS显示的家族聚集模式,使用来自几个已发表的家庭研究的数据。结论:由于IHPS现有家庭数据的一些局限性,本分析结果应谨慎解释。在这些局限性的背景下,发现IHPS先证的同卵双生子和更多远亲之间的家族性复发模式与广义的单主位点遗传不一致。然而,IHPS的家族性复发模式与多因子阈值遗传或多个相互作用位点的影响是相容的。在多基因座相互作用的模型下,没有一个基因座可以解释IHPS先证的一级亲属风险增加超过5倍。与先前的几份报告相反,该分析不支持存在母体因素导致受感染雌性后代患IHPS的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The genetics of infantile hypertrophic pyloric stenosis. A reanalysis.

Objective: To determine whether the existing family data for infantile hypertrophic pyloric stenosis (IHPS) are sufficient for the purposes of establishing the mode of inheritance of this condition.

Design: Reanalysis of the familial aggregation patterns exhibited by IHPS, using data from several published family studies.

Conclusions: Due to several limitations of the available family data for IHPS, the results of this analysis should be interpreted cautiously. Within the context of these limitations, the familial recurrence pattern among monozygotic cotwins and more remote relatives of IHPS probands was found to be inconsistent with generalized single major locus inheritance. The familial recurrence pattern of IHPS is, however, compatible with multifactorial threshold inheritance or the effects of multiple interacting loci. Under a model of multiple interacting loci, no single locus can account for more than a fivefold increase in the risk to first-degree relatives of IHPS probands. In contrast to several earlier reports, this analysis does not support the existence of a maternal factor that contributes to the risk of IHPS in the offspring of affected females.

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