Congenital long QT syndrome

David J. Tester, Peter J. Schwartz, Michael J. Ackerman

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations


With an incidence as high as 1 in 2,000-2,500 live births, long QT syndrome (LQTS) is often characterized clinically by prolongation of the heart rate corrected QT interval (QTc) on a 12-lead surface electrocardiogram (ECG) and is associated with syncope, seizures, and sudden cardiac death due to ventricular arrhythmias usually following a precipitating event such as exertion, extreme emotion, or auditory stimulation. The phenotypic expression of LQTS varies profoundly from asymptomatic longevity to premature sudden cardiac death despite medical therapy. Therefore the clinical/genetic diagnostic evaluation and risk-strati fication are highly important issues in the clinical management of LQTS. This chapter will review the historical background, epidemiology and prevalence, molecular genetics, and clinical presentations of LQTS, explore unique genotype-phenotype relationships that help de fine the various forms of the disorder, and provide a detailed outline for the diagnostic evaluation and clinical management of LQTS patients including current treatment strategies and recommendations.

Original languageEnglish (US)
Title of host publicationElectrical Diseases of the Heart
Subtitle of host publicationVolume 1: Basic Foundations and Primary Electrical Diseases
PublisherSpringer-Verlag London Ltd
Number of pages30
ISBN (Electronic)9781447148814
ISBN (Print)9781447148807
StatePublished - Jan 1 2013


  • Electrocardiogram
  • Genetic testing
  • Genetics
  • Ion channels
  • Long QT syndrome
  • QT interval
  • Sudden death

ASJC Scopus subject areas

  • General Medicine


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