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Syncope in Hereditary Arrhythmogenic Syndromes.

Abstract
Since the discovery of the first mutation causing long QT syndrome (LQTS) in 1995, the field of hereditary arrhythmogenic syndromes has expanded greatly. Today, these syndromes include LQTS, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. There is also evidence suggesting that the newly described malignant early repolarization syndrome also has a genetic cause.
AuthorsArnon Adler, Sami Viskin
JournalCardiology clinics (Cardiol Clin) Vol. 33 Issue 3 Pg. 433-40 (Aug 2015) ISSN: 1558-2264 [Electronic] Netherlands
PMID26115829 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2015 Elsevier Inc. All rights reserved.
Topics
  • Arrhythmias, Cardiac (complications, congenital, genetics)
  • Diagnosis, Differential
  • Electrocardiography
  • Heart Rate (physiology)
  • Humans
  • Risk Factors
  • Syncope (diagnosis, etiology, physiopathology)
  • Syndrome

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