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.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Cardiology |
| Vol/bind | 115 |
| Udgave nummer | 4 |
| Sider (fra-til) | 311-6 |
| Antal sider | 6 |
| ISSN | 0008-6312 |
| DOI | |
| Status | Udgivet - 1 jan. 2010 |
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