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T-wave patterns associated with the hereditary long QT syndrome
1Department of Medicine, Division of Cardiology, University of Rochester Medical Center, Rochester, New York, USA. heartajm@heart.rochester.edu
Abstract:
Mutations involving 6 different ion-channel genes have been identified in subjects with the hereditary Long QT Syndrome. These gene mutations result in structural and functional changes in ion-channel proteins with resultant alterations in potassium and sodium repolarization currents that affect the morphologic features of electrocardiographic repolarization. This review highlights the genotype-phenotype associations related to ventricular repolarization that have been reported in the LQTS literature, with particular focus on ECG T-wave patterns in LQT1, LQT2, and LQT3 genotypes.