Electrocardiographic characteristics of ventricular arrhythmia in inherited channelopathies

Nilubon Methachittiphan, Peerawut Deeprasertkul, Mark S. Link

Research output: Contribution to journalReview article

Abstract

Ventricular arrhythmias in structurally normal hearts can be divided into idiopathic ventricular arrhythmia, in which there is no known ion mutation or genetic component, and inherited ion channelopathies, in which gene mutations causing ion-channel dysfunction play an important role in the mechanism of ventricular arrhythmia. Inherited channelopathies are Long QT syndrome, Short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. Recognizing ECG patterns of these arrhythmias is important because they can cause sudden cardiac deaths that are preventable with defibrillator implantations.

Original languageEnglish (US)
Pages (from-to)419-432
Number of pages14
JournalCardiac Electrophysiology Clinics
Volume6
Issue number3
DOIs
StatePublished - Sep 2014

Keywords

  • Brugada syndrome
  • Catecholaminergic polymorphic ventricular tachycardia
  • Long-QT syndrome
  • Short-QT syndrome
  • Ventricular fibrillation

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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