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A Familial 7q36.3 Duplication Associated with Agenesis of the Corpus Callosum

机译:与q体发育不全相关的家族性7q36.3复制。

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摘要

Small chromosomal duplications involving 7q36.3 have rarely been reported. This clinical report describes four individuals from a three-generation family with agenesis of the corpus callosum (ACC) and a 0.73 Mb duplication of 7q36.3 detected by array CGH. The 7q36.3 duplication involves two genes: RNA Binding Motif Protein 33 (RBM33) and Sonic Hedgehog (SHH). Most affected family members had mild intellectual disability or borderline intellectual functioning, macrocephaly, a broad forehead, and widely spaced eyes. Two individuals had a Chiari type I malformation. This is the first family reported with ACC associated with a small duplication of these genes. While we cannot establish causation for the relationship between any single gene and the ACC in this family, there is a role for SHH in the formation of the corpus callosum through correct patterning and assembly of the commissural plate, and these data concur with vertebrate studies showing that a gain of SHH expands the facial primordium. (C) 2015 Wiley Periodicals, Inc.
机译:很少报道涉及7q36.3的小染色体重复。该临床报告描述了来自三代家庭的四​​名个体,其call体发育不全(ACC),阵列CGH检测到7q36.3的0.73 Mb重复。 7q36.3复制涉及两个基因:RNA结合基序蛋白33(RBM33)和声波刺猬(SHH)。大多数受影响的家庭成员患有轻度智力残疾或边缘性智力功能,大头畸形,额头宽大且眼睛间距大。两个人患有Chiari I型畸形。这是第一个报告的与ACC相关的家族,与这些基因的少量重复有关。虽然我们无法确定该家族中任何单个基因与ACC之间的关系有因果关系,但SHH在通过正确的连合板构图和组装而在call体形成中发挥了作用,这些数据与脊椎动物研究一致SHH的获得会扩大面部原基。 (C)2015年Wiley Periodicals,Inc.

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