Introduction: Congenital long QT syndrome (LQTS) is a cardiac ion channelopathy that
predisposes affected individuals to spontaneous ventricular tachycardia/fibrillation (VT/VF) …

Background: Long QT syndrome (LQTS) is a rare genetic disorder and a major preventable
cause of sudden cardiac death in the young. A causal rare genetic variant with large effect …

Importance Long QT syndrome (LQTS) is caused by several ion channel genes, yet risk of
arrhythmic events is not determined solely by the responsible gene pathogenic variants …

Objectives: Genetic testing, a gold standard for long QT syndrome (LQTS) diagnosis, is time-
consuming and costly when all the 15 candidate genes are screened. Since genotype …

Importance Congenital long QT syndrome (LQTS) is associated with syncope, ventricular
arrhythmias, and sudden death. Half of patients with LQTS have a normal or borderline …

Long QT syndrome (LQTS) is an inherited (autosomal dominant) channelopathy associated
with susceptibility to ventricular arrhythmias due to malfunction of ion channels in …

Background—Inherited long-QT syndrome (LQTS) is associated with risk of sudden death.
We assessed the clinical course and the fulfillment of current treatment strategies in …

Background We aimed to provide personalized risk estimates for cardiac events (CEs) and
life‐threatening events in women with either type 1 or type 2 long QT. Methods and Results …

Abstract Background: Long QT syndrome (LQTS) is a common inheritable arrhythmogenic
disorder, often secondary to mutations in the KCNQ1, KCNH2, and SCN5A genes. The …

Introduction Long QT syndrome (LQTS) is a less prevalent cardiac ion channelopathy than
Brugada syndrome in Asia. The present study compared the outcomes between …