Long QT syndrome (LQTS) is an inherited primary arrhythmia syndrome that may present
with malignant arrhythmia and, rarely, risk of sudden death. The clinical symptoms include …

Long QT syndrome (LQTS) is caused by functional alterations in cardiac ion channels and is
associated with prolonged cardiac repolarization time and increased risk of ventricular …

LQTS as a Paradigm. The inherited long QT syndrome (LQTS) is a familial disease
characterized by QT interval changes that often are labile, syncope, and sudden death due …

The congenital long QT syndrome is a rare disorder in which mutation carriers are at risk for
polymorphic ventricular tachycardia and/or sudden cardiac death. Discovery and analysis of …

The hereditary Long QT syndrome (LQTS) is a genetic channelopathy with variable
penetrance that is associated with increased propensity for polymorphic ventricular …

Aims Congenital long QT syndromes (LQTSs) are associated with prolonged ventricular
repolarization and sudden cardiac death. Limitations to existing clinical therapeutic …

Long QT syndrome (LQTS) is a cardiac electrophysiologic disorder, characterized by QT
prolongation and T-wave abnormalities on the EKG that are associated with …

Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval
prolongation and life-threatening arrhythmias, leading to syncope and sudden death …

The long QT syndrome (LQTS) is a disorder of cardiac ion channels that affect
repolarization. The characteristic manifestations are prolongation of the QT interval and T …

Background Long-QT syndromes are heritable diseases associated with prolongation of the
QT interval on an electrocardiogram and a high risk of sudden cardiac death due to …