Literature DB >> 11265709

Genetics of brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes.

J A Towbin1, M Vatta, H Li.   

Abstract

This article outlines the up-to-date understanding of the molecular basis of primary ventricular arrhythmias. Two disorders have recently been well described at the molecular level, the long QT syndromes and Brugada syndrome, and this article reviews the current scientific knowledge of each disease. A third disorder, arrhythmogenic right ventricular dysplasia, which is on the cusp of understanding, will also be described.

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Year:  2000        PMID: 11265709     DOI: 10.1054/jelc.2000.20361

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  3 in total

Review 1.  Arrhythmogenic right ventricular dysplasia/cardiomyopathy: new avenues for diagnosis and treatment.

Authors:  E E van der Wall; M Bootsma; H J J Wellens; J J Bax; A de Roos; M J Schalij
Journal:  Neth Heart J       Date:  2003-01       Impact factor: 2.380

2.  Case report: fatal ventricular tachycardia exacerbated by fever in a child.

Authors:  A Miyazaki; Y Ono; C Yutani; S Echigo
Journal:  Pediatr Cardiol       Date:  2004-06-08       Impact factor: 1.655

3.  Coexistent Brugada Syndrome and Wolff-Parkinson-White Syndrome: What is the Optimal Management?

Authors:  Abhishek Jaiswal; Katherine Heretis; Seth Goldbarg
Journal:  Indian Pacing Electrophysiol J       Date:  2013-09-01
  3 in total

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