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21三体对面部形态及变异性的影响。

The Influence of trisomy 21 on facial form and variability.

作者信息

Starbuck John M, Cole Theodore M, Reeves Roger H, Richtsmeier Joan T

机构信息

Department of Anthropology, University of Central Florida, Orlando, Florida.

Department of Biomedical Sciences, School of Medicine, University of Missouri-Kansas City, Kansas City, Missouri.

出版信息

Am J Med Genet A. 2017 Nov;173(11):2861-2872. doi: 10.1002/ajmg.a.38464. Epub 2017 Sep 21.

Abstract

Triplication of chromosome 21 (trisomy 21) results in Down syndrome (DS), the most common live-born human aneuploidy. Individuals with DS have a unique facial appearance that can include form changes and altered variability. Using 3D photogrammatic images, 3D coordinate locations of 20 anatomical landmarks, and Euclidean Distance Matrix Analysis methods, we quantitatively test the hypothesis that children with DS (n = 55) exhibit facial form and variance differences relative to two different age-matched (4-12 years) control samples of euploid individuals: biological siblings of individuals with DS (n = 55) and euploid individuals without a sibling with DS (n = 55). Approximately 36% of measurements differ significantly between DS and DS-sibling samples, whereas 46% differ significantly between DS and unrelated control samples. Nearly 14% of measurements differ significantly in variance between DS and DS sibling samples, while 18% of measurements differ significantly in variance between DS and unrelated euploid control samples. Of those measures that showed a significant difference in variance, all were relatively increased in the sample of DS individuals. These results indicate that faces of children with DS are quantitatively more similar to their siblings than to unrelated euploid individuals and exhibit consistent, but slightly increased variation with most individuals falling within the range of normal variation established by euploid samples. These observations provide indirect evidence of the strength of the genetic underpinnings of the resemblance between relatives and the resistance of craniofacial development to genetic perturbations caused by trisomy 21, while underscoring the complexity of the genotype-phenotype map.

摘要

21号染色体三体性(21三体)导致唐氏综合征(DS),这是最常见的活产人类非整倍体疾病。患有唐氏综合征的个体具有独特的面部外观,可能包括形态变化和变异性改变。我们使用三维摄影图像、20个解剖学标志点的三维坐标位置以及欧氏距离矩阵分析方法,定量检验了以下假设:唐氏综合征患儿(n = 55)与两个不同的年龄匹配(4至12岁)的整倍体个体对照样本相比,面部形态和变异性存在差异,这两个对照样本分别是:唐氏综合征个体的生物学兄弟姐妹(n = 55)以及没有唐氏综合征兄弟姐妹的整倍体个体(n = 55)。唐氏综合征样本与唐氏综合征患儿的兄弟姐妹样本之间约36%的测量值存在显著差异,而唐氏综合征样本与无血缘关系的对照样本之间46%的测量值存在显著差异。唐氏综合征样本与唐氏综合征患儿的兄弟姐妹样本之间近14%的测量值在变异性上存在显著差异,而唐氏综合征样本与无血缘关系的整倍体对照样本之间18%的测量值在变异性上存在显著差异。在那些变异性存在显著差异的测量值中,所有测量值在唐氏综合征个体样本中都相对增加。这些结果表明,唐氏综合征患儿的面部在数量上与其兄弟姐妹比与无血缘关系的整倍体个体更相似,并且表现出一致但略有增加的变异性,大多数个体落在整倍体样本确定的正常变异范围内。这些观察结果间接证明了亲属之间相似性的遗传基础的强度以及颅面发育对21三体引起的遗传扰动的抵抗力,同时强调了基因型-表型图谱的复杂性。

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4
Embryonic bauplans and the developmental origins of facial diversity and constraint.
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6
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