| Literature DB >> 25944787 |
Keith Wong1, Randal Moldrich2, Matthew Hunter1,3, Matthew Edwards4, David Finlay5, Sheridan O'Donnell3, Tom MacDougall6, Nicole Bain7, Benjamin Kamien1,3.
Abstract
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.Entities:
Keywords: Chiari malformation; RBM33; SHH; agenesis of the corpus callosum; chromosome 7q36.3; macrocephaly; sonic hedgehog
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Year: 2015 PMID: 25944787 DOI: 10.1002/ajmg.a.37143
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802