We report an idiopathic variant of the long QT syndrome in a 72 year old woman with a
history of recurrent syncope over 3 years who presented with repeated episodes of cardiac …

Long-QT syndrome is a rare, inherited cardiac channelopathy that is characterized by
arrhythmia, syncope and sudden cardiac death. Foetal symptoms are very rare and prenatal …

Long QT syndrome (LQT) and WPW syndrome are causes of sudden cardiac death (SCD) in
the young, and their association has been rarely reported. A 26-year-old woman presented …

Congenital Long QT Syndrome (LQTS) is a dangerous arrhythmic disorder that can be
diagnosed in children with bradycardia. It is characterised by a prolonged QT interval and …

Congenital long QT syndrome is an inherited disorder of cardiac repolarization that
predisposes to syncope and to sudden death from polymorphic ventricular tachycardia. The …

Background and Objectives Congenital long QT syndrome (LQTS) is characterized by the
prolongation of the QT interval, frequent episodes of syncope and Torsades de Pointes …

Long QT syndrome (LQTS) is an ion channelopathy that may cause life-threatening
ventricular arrhythmias resulting in intrauterine death, cardiac arrest, or sudden death at any …

The congenital long QT syndrome was first described in individuals with structurally normal
hearts in 1957. 1 Little was known about the significance of a short QT interval. In 1993, after …

Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome
characterized by a lengthening of the QT interval on the surface ECG and a propensity to …