| Literature DB >> 26197979 |
Loubna Jouan1, Bouchra Ouled Amar Bencheikh1, Hussein Daoud1, Alexandre Dionne-Laporte1, Sylvia Dobrzeniecka1, Dan Spiegelman1, Daniel Rochefort1, Pascale Hince1, Anna Szuto1, Maryse Lassonde2,3, Marine Barbelanne4,5, William Y Tsang4,5,6, Patrick A Dion1,4, Hugo Théoret2,3, Guy A Rouleau1.
Abstract
Agenesis of the corpus callosum (ACC) is a common brain malformation which can be observed either as an isolated condition or as part of numerous congenital syndromes. Therefore, cognitive and neurological involvements in patients with ACC are variable, from mild linguistic and behavioral impairments to more severe neurological deficits. To date, the underlying genetic causes of isolated ACC remains elusive and causative genes have yet to be identified. We performed exome sequencing on three acallosal siblings from the same non-consanguineous family and identified compound heterozygous variants, p.[Gly94Arg];[Asn1232Ser], in the protein encoded by the CDK5RAP2 gene, also known as MCPH3, a gene previously reported to cause autosomal recessive primary microcephaly. Our findings suggest a novel role for this gene in the pathogenesis of isolated ACC.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26197979 PMCID: PMC4929875 DOI: 10.1038/ejhg.2015.156
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246