| Literature DB >> 20395683 |
Anders G Holst1, Bo Liang, Thomas Jespersen, Henning Bundgaard, Stig Haunso, Jesper Hastrup Svendsen, Jacob Tfelt-Hansen.
Abstract
Mutations in the cardiac sodium channel encoded by the gene SCN5A can result in a wide array of phenotypes. We report a case of a young male with a novel SCN5A mutation (R121W) afflicted by sick sinus syndrome, progressive cardiac conduction disorder, atrial flutter and ventricular tachycardia. His father carried the same mutation, but had a milder phenotype, presenting with progressive cardiac conduction later in life. The mutation was found to result in a loss-of-function in the sodium current. In conclusion, the same SCN5A mutation can result in a wide array of clinical phenotypes and perhaps the spectrum of SCN5A loss-of-function associated disease entities should be viewed as one syndrome. Copyright (c) 2010 S. Karger AG, Basel.Entities:
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Year: 2010 PMID: 20395683 DOI: 10.1159/000312747
Source DB: PubMed Journal: Cardiology ISSN: 0008-6312 Impact factor: 1.869