| Literature DB >> 24176758 |
Catherine A Brownstein1, Meghan C Towne, Lovelace J Luquette, David J Harris, Nicholas S Marinakis, Peter Meinecke, Kerstin Kutsche, Philippe M Campeau, Timothy W Yu, David M Margulies, Pankaj B Agrawal, Alan H Beggs.
Abstract
KCNJ8 (NM_004982) encodes the pore forming subunit of one of the ATP-sensitive inwardly rectifying potassium (KATP) channels. KCNJ8 sequence variations are traditionally associated with J-wave syndromes, involving ventricular fibrillation and sudden cardiac death. Recently, the KATP gene ABCC9 (SUR2, NM_020297) has been associated with the multi-organ disorder Cantú syndrome or hypertrichotic osteochondrodysplasia (MIM 239850) (hypertrichosis, macrosomia, osteochondrodysplasia, and cardiomegaly). Here, we report on a patient with a de novo nonsynonymous KCNJ8 SNV (p.V65M) and Cantú syndrome, who tested negative for mutations in ABCC9. The genotype and multi-organ abnormalities of this patient are reviewed. A careful screening of the KATP genes should be performed in all individuals diagnosed with Cantú syndrome and no mutation in ABCC9.Entities:
Keywords: Cantú syndrome; Exome; Mutation; Potassium channel
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Year: 2013 PMID: 24176758 PMCID: PMC3902017 DOI: 10.1016/j.ejmg.2013.09.009
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708