Abstract The Short QT Syndrome is a recently described new genetic disorder, characterized
by abnormally short QT interval, paroxysmal atrial fibrillation and life threatening ventricular …

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 …

The short QT syndrome is a new congenital entity associated with familial atrial fibrillation
and/or sudden death or syncope. Three different gain-of-function mutations in genes …

Congenital or familial short QT syndrome is a genetically heterogeneous cardiac
channelopathy without structural heart disease that has a dominant autosomal or sporadic …

Objectives: The purpose of this study was to evaluate the efficacy of various antiarrhythmic
drugs at prolonging the QT interval into the normal range and preventing ventricular …

Short QT syndrome (SQTS) is a gene-related arrhythmogenic syndrome harbouring a large
spectrum of symptoms ranging from mild palpitations to sudden cardiac death. The mutation …

There are many cardiac arrhythmias and sudden cardiac death (SCD) related to
channelopathies or ion channel disorders. Short QT syndrome (SQTS) is an inherited …

There are many diseases related to ion‐channel disorders, so‐called “channelopathies.”
Hereditary short QT syndrome is a clinical‐electrocardiographic entity with autosomal …

Short QT syndrome (SQTS) is one of the rarest inheritable cardiac channelopathies,
characterized by an accelerated cardiac repolarization, which is also the substrate for the …

The short QT syndrome constitutes a new clinical entity that is associated with a high
incidence of sudden cardiac death, syncope, and/or atrial fibrillation even in young patients …