Genetics of nonsyndromic cleft lip with or without cleft palate: is there a Mendelian sub-entity?

Vincent Gajdos , Michel Bahuau , Elisabeth Robert-Gnansia , Christine Francannet , Sylvaine Cordier , Catherine Bonaïti-Pellié
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引用次数: 3

Abstract

The mode of inheritance of nonsyndromic cleft lip with or without cleft palate (NSCLP) is still a matter of dispute. We performed segregation analysis on three data sets of families ascertained through an affected child with NSCLP. The first two data sets were selected in France and were pooled for a global analysis. No major gene effect could be evidenced in spite of a very large number of families (666 pedigrees including 719 nuclear families). The third data set was British and consisted of three-generation families including the offspring of probands. A major gene effect, as well as a strong residual multifactorial component, were highly significant and we could show that this evidence almost entirely came from the information on probands’ offspring. We conclude that a mixture of monogenic and of multifactorial cases is probably the best explanation for the observations made in this study. Analyses performed in pedigrees with multiple cases closely related might allow reducing heterogeneity and help identifying those Mendelian sub-entities.

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非综合征性唇裂伴或不伴腭裂的遗传学:是否存在孟德尔子实体?
非综合征性唇裂伴或不伴腭裂(NSCLP)的遗传方式仍存在争议。我们对三组通过非小细胞肺癌患儿确定的家庭数据进行了分离分析。前两个数据集是在法国选定的,并汇集在一起进行全球分析。尽管有大量的家庭(666个谱系,包括719个核心家庭),但没有主要的基因效应可以证明。第三组数据来自英国,由包括先证者后代在内的三代家庭组成。一个主要的基因效应,以及一个强大的残余多因子成分,是非常显著的,我们可以表明,这一证据几乎完全来自先证者的后代的信息。我们的结论是,单基因和多因子病例的混合可能是本研究中观察到的最好解释。在有多个密切相关病例的谱系中进行的分析可能会减少异质性,并有助于识别孟德尔子实体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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