A 31-year-old woman with congenital long QT syndrome (LQTS) underwent dual-chamber
ICD implantation at 21 years of age for recurrent syncope. Her corrected QT interval (QTc) …

Congenital long QT syndrome (LQTS) is an inherited cardiac disease characterized by a
prolonged QT interval and ventricular arrhythmias such as ventricular fibrillation or …

OBJECTIVES: The purpose of this study was to evaluate retrospectively a single-center
experience with the use of ICDs in patients with long QT syndrome (LQTS) concerning …

Congenital long QT syndrome (LQTS) can present as syncope or seizures, secondary to
polymorphic ventricular tachycardia, mimicking a primary seizure disorder. In patients …

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 …

The short QT syndrome is a new congenital entity associated with familial atrial fibrillation
and/or sudden death or syncope occurring in all age groups, even in newborns. The …

Congenital long QT syndrome (LQT) is a potentially lethal hereditary arrhythmic disorder that
can cause syncope and sudden cardiac death owing to polymorphic ventricular …

Four patients with long QT type 2, aged 11 to 18 years from unrelated families, with recurrent
syncope and polymorhic ventricular tachycardia were studied. Long QT syndrome was …

Short QT syndrome is a new inherited disorder associated with familial atrial fibrillation
and/or sudden death or syncope. To date, three different mutations in genes encoding …