A familial 7q36.3 duplication associated with agenesis of the corpus callosum

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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 0.73Mb 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.

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Wong, K., Moldrich, R., Hunter, M., Edwards, M., Finlay, D., O’Donnell, S., … Kamien, B. (2015). A familial 7q36.3 duplication associated with agenesis of the corpus callosum. American Journal of Medical Genetics, Part A, 167(9), 2201–2208. https://doi.org/10.1002/ajmg.a.37143

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