| Literature DB >> 19365654 |
Juan Villafane1, Ming Lon Young, Philippe Maury, Christian Wolpert, Olli Anttonen, Robert Hamilton, Prince J Kannankeril, Peter S Fischbach.
Abstract
Short QT syndrome (SQTS) is a recently described genetic syndrome characterized by abnormally brisk ventricular repolarization. Similar to long QT syndrome, SQTS might result in ventricular arrhythmias, syncope, and sudden death. The clinical diagnosis of SQTS is supported by the finding of an abnormally short QT interval on the resting electrocardiogram in combination with a suggestive clinical or family history. To date, few pediatric cases have been reported and the ideal therapy is unknown. We report a teenage boy who suffered a witnessed ventricular fibrillation arrest and was subsequently diagnosed with SQTS. Additional data from nine other pediatric patients diagnosed with SQTS are presented.Entities:
Mesh:
Year: 2009 PMID: 19365654 DOI: 10.1007/s00246-009-9439-9
Source DB: PubMed Journal: Pediatr Cardiol ISSN: 0172-0643 Impact factor: 1.655