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下颌前突的主基因和多基因遗传

Major gene and multifactorial inheritance of mandibular prognathism.

作者信息

Cruz Ricardo Machado, Krieger Henrique, Ferreira Ricardo, Mah James, Hartsfield James, Oliveira Silviene

机构信息

Departament of Genetics and Morphology, University of Brasília, Brasília, DF, Brazil.

出版信息

Am J Med Genet A. 2008 Jan 1;146A(1):71-7. doi: 10.1002/ajmg.a.32062.

Abstract

Mandibular prognathism typically shows familial aggregation. Various genetic models have been described and it is assumed to be a multifactorial and polygenic trait, with a threshold for expression. Our goal was to examine specific genetic models of the familial transmission of this trait. The study sample comprised of 2,562 individuals from 55 families. Complete family histories for each proband were ascertained and the affection status of relatives were confirmed by lateral cephalograms, photographs, and dental models. Pedigrees were drawn using PELICAN and complex segregation analysis was performed using POINTER. Parts of some pedigrees were excluded to create one founder pedigrees, so the total N was 2,050. Analysis showed more affected females than males (P = 0.030). The majority of the pedigrees suggest autosomal dominant inheritance. Incomplete penetrance was demonstrated by the ratio of affected/unaffected parents and siblings. The heritability of mandibular prognathism was estimated to be 0.316. We conclude that there is a major gene that influences the expression of mandibular prognathism with clear signs of Mendelian inheritance and a multifactorial component.

摘要

下颌前突通常呈现家族聚集性。已经描述了多种遗传模式,并且假定它是一种多因素和多基因性状,具有表达阈值。我们的目标是研究该性状家族传递的特定遗传模式。研究样本包括来自55个家庭的2562名个体。确定了每个先证者的完整家族史,并通过头颅侧位片、照片和牙模确认了亲属的患病状况。使用PELICAN绘制系谱图,并使用POINTER进行复杂分离分析。排除了一些系谱的部分内容以创建一个奠基者系谱,因此总数N为2050。分析显示,受影响的女性多于男性(P = 0.030)。大多数系谱表明为常染色体显性遗传。通过受影响/未受影响的父母和兄弟姐妹的比例证明了不完全外显率。下颌前突的遗传度估计为0.316。我们得出结论,存在一个主要基因影响下颌前突的表达,具有明显的孟德尔遗传迹象和多因素成分。

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