Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are
associated with cardiac repolarization dysfunction. Since its initial description in 1957, our …

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

Congenital long QT syndrome (LQTS) is a rare but potentially lethal disease, characterized
by prolongation of QT interval, recurrent syncope, and sudden death. In the pregenomic era …

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

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 …

The long QT syndrome (LQTS) is a genetic disorder characterized by prolongation of the QT
interval in the electrocardiogram (ECG) and a propensity to torsades de pointes ventricular …

Objectives: We sought to assess the spectrum and outcome of young long QT syndrome
(LQTS) patients, addressing treatment including device indications, risks, and benefits …

BACKGROUND: Long QT syndrome's (LQTS) marked heterogeneity necessitates both
evidence-based and individualized therapeutic approaches. OBJECTIVE: This study sought …

Short QT syndrome (SQTS) is an inheritable primary electric disease of the heart
characterized by abnormally short QT intervals on the ECG and an increased propensity to …

Short QT syndrome is an inheritable primary electrical disease of the heart that was
discovered in 1999. The disorder is characterized by an abnormally short QT interval (< 300 …