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本文引用的文献

1
Atypical face shape and genomic structural variants in epilepsy.癫痫症中的非典型面型和基因组结构变异。
Brain. 2012 Oct;135(Pt 10):3101-14. doi: 10.1093/brain/aws232. Epub 2012 Sep 13.
2
Ethanol-induced face-brain dysmorphology patterns are correlative and exposure-stage dependent.乙醇诱导的面-脑畸形模式具有相关性和暴露阶段依赖性。
PLoS One. 2012;7(8):e43067. doi: 10.1371/journal.pone.0043067. Epub 2012 Aug 22.
3
The face signature of fibrodysplasia ossificans progressiva.进行性骨化性纤维发育不良的面部特征。
Am J Med Genet A. 2012 Jun;158A(6):1368-80. doi: 10.1002/ajmg.a.35346. Epub 2012 May 11.
4
Large-scale objective phenotyping of 3D facial morphology.大规模客观的 3D 面部形态分析。
Hum Mutat. 2012 May;33(5):817-25. doi: 10.1002/humu.22054. Epub 2012 Mar 20.
5
Another cause of vaccine encephalopathy: a case of Angelman syndrome.疫苗性脑病的另一个病因:1例天使综合征病例。
Eur J Med Genet. 2012 May;55(5):338-41. doi: 10.1016/j.ejmg.2012.01.008. Epub 2012 Jan 25.
6
Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome.精细的面部表型-基因型分析在 Wolf-Hirschhorn 综合征中。
Eur J Hum Genet. 2012 Jan;20(1):33-40. doi: 10.1038/ejhg.2011.135. Epub 2011 Jul 27.
7
Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging.脆性 X 综合征小鼠模型的磁共振成像解剖表型分析。
Neuroimage. 2010 Nov 15;53(3):1023-9. doi: 10.1016/j.neuroimage.2010.03.038. Epub 2010 Mar 19.
8
FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development.FMR1/FXR1 和 miRNA 通路对于眼睛和神经嵴发育是必需的。
Dev Biol. 2010 May 1;341(1):222-35. doi: 10.1016/j.ydbio.2010.02.031. Epub 2010 Mar 1.
9
Generation and characterization of FMR1 knockout zebrafish.FMR1 敲除斑马鱼的产生和特性分析。
PLoS One. 2009 Nov 19;4(11):e7910. doi: 10.1371/journal.pone.0007910.
10
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome.神经嵴迁移的抑制是巴德-比德尔综合征中颅面畸形和先天性巨结肠病的基础。
Proc Natl Acad Sci U S A. 2008 May 6;105(18):6714-9. doi: 10.1073/pnas.0707057105. Epub 2008 Apr 28.

脆性 X 综合征在人和小鼠中的颅面特征。

Craniofacial characteristics of fragile X syndrome in mouse and man.

机构信息

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

出版信息

Eur J Hum Genet. 2013 Aug;21(8):816-23. doi: 10.1038/ejhg.2012.265. Epub 2012 Dec 5.

DOI:10.1038/ejhg.2012.265
PMID:23211703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3722676/
Abstract

For a disorder as common as fragile X syndrome, the most common hereditary form of cognitive impairment, the facial features are relatively ill defined. An elongated face and prominent ears are the most commonly accepted dysmorphic hallmarks. We analysed 3D facial photographs of 51 males and 15 females with full FMR1 mutations and 9 females with a premutation using dense-surface modelling techniques and a new technique that forms a directed graph with normalized face shapes as nodes and edges linking those with closest dysmorphism. In addition to reconfirming known features, we confirmed the occurrence of some at an earlier age than previously recorded. We also identified as yet unrecorded facial characteristics such as reduced facial depth, hypoplasticity of the nasal bone-cartilage interface and narrow mid-facial width exaggerating ear prominence. As no consistent craniofacial abnormalities had been reported in animal models, we analysed micro-CT images of the fragile X mouse model. Results indicated altered dimensions in the mandible and both outer and inner skull, with the latter potentially reflecting differences in neuroanatomy. We extrapolated the mouse results to face shape differences of the human fragile X face.

摘要

对于脆性 X 综合征这种常见的认知障碍遗传性疾病(最常见的类型),其面部特征相对不明确。长脸和大耳朵是最常见的公认的畸形特征。我们使用密集表面建模技术和一种新的技术,将归一化的面部形状作为节点形成有向图,将具有最接近畸形的节点连接起来,分析了 51 名男性和 15 名女性的全 FMR1 突变和 9 名女性前突变的 3D 面部照片。除了重新确认已知的特征外,我们还确认了一些以前记录中更早出现的特征。我们还确定了一些尚未记录的面部特征,如面部深度减小、鼻骨-软骨界面发育不全以及中面部宽度变窄,使耳朵更加突出。由于在动物模型中没有报告一致的颅面异常,我们分析了脆性 X 小鼠模型的 micro-CT 图像。结果表明下颌骨和内外颅骨的尺寸发生了改变,后者可能反映了神经解剖学的差异。我们推断出小鼠结果与人类脆性 X 面部的面部形状差异。