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Translational genetic modelling of 3D craniofacial dysmorphology: elaborating the facial phenotype of neurodevelopmental disorders through the prism of schizophrenia

机译:三维颅面畸形的转化遗传建模:通过精神分裂症的棱镜阐述神经发育障碍的面部表型

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摘要

Purpose of Review: ududIn the context of human developmental conditions, we review the conceptualisation of schizophrenia as a neurodevelopmental disorder, the status of craniofacial dysmorphology as a clinically accessible index of brain dysmorphogenesis, the ability of genetically modified mouse models of craniofacial dysmorphology to inform on the underlying dysmorphogenic process and how geometric morphometric techniques in mutant mice can extend quantitative analysis.ududRecent Findings: ududMutant mice with disruption of neuregulin-1, a gene associated meta-analytically with risk for schizophrenia, constitute proof-of-concept studies of murine facial dysmorphology in a manner analogous to clinical studies in schizophrenia. Geometric morphometric techniques informed on the topography of facial dysmorphology and identified asymmetry therein.ududSummary: ududTargeted disruption in mice of genes involved in individual components of developmental processes and analysis of resultant facial dysmorphology using geometric morphometrics can inform on mechanisms of dysmorphogenesis at levels of incisiveness not possible in human subjects.
机译:审查目的: ud ud在人类发育状况的背景下,我们回顾了精神分裂症作为一种神经发育障碍的概念,颅面畸形的临床状况,脑畸形发生的指标,遗传修饰的颅面畸形小鼠模型的能力目的在于了解潜在的畸形发生过程以及突变小鼠的几何形态计量学技术如何可以扩展定量分析。 ud ud最近的发现: ud ud突变的小鼠神经调节蛋白-1(一种通过基因分析与精神分裂症相关的基因被破坏)构成小鼠面部畸形的概念验证研究,类似于精神分裂症的临床研究。几何形态计量学技术可告知面部畸形的形貌,并在其中识别出不对称性。 ud ud摘要: ud ud针对小鼠中涉及发育过程各个组成部分的基因的破坏以及使用几何形态计量学对所得面部畸形的分析可以为机理提供依据在人类受试者中不可能达到尖锐程度的畸形发生。

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