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非综合征性唇腭裂的复杂分离分析。

Complex segregation analysis of nonsyndromic cleft lip and palate.

作者信息

Hecht J T, Yang P, Michels V V, Buetow K H

机构信息

Department of Pediatrics, University of Texas Medical School, Houston 77225.

出版信息

Am J Hum Genet. 1991 Sep;49(3):674-81.

Abstract

This study was undertaken to examine the inheritance pattern of nonsyndromic cleft lip with or without cleft palate (CL/P). Complex segregation analysis using the unified model as in POINTER and the regressive model as in REGD programs were applied to analyze a midwestern U.S. Caucasian population of 79 families ascertained through a proband with CL/F. In REGD, the dominant or codominant Mendelian major locus models of inheritance were the most parsimonious fit. In POINTER, besides the Mendelian major locus model, the multifactorial threshold (MF/T) model and the mixed model were also consistent with the observed data. However, the high heritability parameter of .93 (SD .063) in the MF/T model suggests that any random exogenous factors are unlikely to be the underlying mechanisms, and the mixed model indicates that this high heritability is accounted for by a major dominant locus component. These findings indicate that the best explanation for the etiology of CL/P in this study population is a putative major locus associated with markedly decreased penetrance. Molecular studies may provide further insight into the genetic mechanism underlying CL/P.

摘要

本研究旨在探讨非综合征性唇裂伴或不伴腭裂(CL/P)的遗传模式。采用POINTER中的统一模型和REGD程序中的回归模型进行复杂分离分析,以分析通过CL/F先证者确定的美国中西部白种人79个家庭。在REGD中,显性或共显性孟德尔主要基因座遗传模型是最简约的拟合。在POINTER中,除了孟德尔主要基因座模型外,多因素阈值(MF/T)模型和混合模型也与观察数据一致。然而,MF/T模型中0.93(标准差0.063)的高遗传度参数表明,任何随机的外源性因素不太可能是潜在机制,混合模型表明这种高遗传度是由一个主要显性基因座成分造成的。这些发现表明,本研究人群中CL/P病因的最佳解释是一个假定的主要基因座,其外显率明显降低。分子研究可能会进一步深入了解CL/P的遗传机制。

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