New Revelations about the Long-QT Syndrome
- 10 August 1995
- journal article
- review article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 333 (6) , 384-385
- https://doi.org/10.1056/nejm199508103330613
Abstract
Sudden death, a devastating event for any family, strikes more than 300,000 Americans each year. Cardiac arrhythmias, particularly ventricular arrhythmias, are thought to account for about 11 percent of all sudden deaths. In some cases there appears to be a familial propensity for sudden death. One inherited condition, the Romano–Ward long-QT syndrome, is an autosomal dominant disorder of cardiac repolarization that results in ventricular arrhythmias and sudden death. The long-QT syndrome has been thought to arise from either an abnormality of ion-channel regulation (the myocellular hypothesis) or altered activity of the autonomic nervous system, but definitive proof of either hypothesis . . .Keywords
This publication has 5 references indexed in Scilit:
- A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channelCell, 1995
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneityNature Genetics, 1994
- Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 GeneScience, 1991