SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolarization, a predisposition to atrial and ventricular fibrillatory arrhythmias, and a risk of sudden death. Few cases have been reported, but the prevalence may be underestimated. This syndrome might account for some cases of unexplained ventricular fibrillation in patients with otherwise healthy hearts. Patients have abnormally short QT intervals and refractory periods, and atrial/ventricular fibrillation can be triggered during investigations. Gain-of-function mutations have been detected in three genes encoding potassium channels. Treatment is based on defibrillator implantation, sometimes as a preventive measure. Quinidine may be beneficial...
The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abno...
Background: Some congenital heart conditions are very rare. In a climate of limited resources, a vie...
Short QT syndrome (SQTS) is an extremely rare inherited arrhythmogenic entity. Nowadays, less than 2...
SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolar...
The short QT syndrome (SQTS) is a new member of the genetic arrhythmia family (including long QT syn...
Short QT syndrome is a highly malignant inherited cardiac disease characterized by ventricular tachy...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
ObjectivesThe aim of this study was to investigate the clinical characteristics and the long-term co...
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy withou...
Congenital disorders of cardiac repolarization are associated with risk of serious arrhythmias and s...
The short QT syndrome (SQTS) is a recently described genetic arrhythmogenic disorder, characterized ...
ObjectivesWe aimed to develop diagnostic criteria for the short QT syndrome (SQTS) to facilitate cli...
Short QT syndrome (SQTS) is one of the rarest inheritable cardiac channelopathies, characterized by ...
ObjectivesThis study intends to gain further insights into the natural history, the yield of familia...
The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abno...
Background: Some congenital heart conditions are very rare. In a climate of limited resources, a vie...
Short QT syndrome (SQTS) is an extremely rare inherited arrhythmogenic entity. Nowadays, less than 2...
SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolar...
The short QT syndrome (SQTS) is a new member of the genetic arrhythmia family (including long QT syn...
Short QT syndrome is a highly malignant inherited cardiac disease characterized by ventricular tachy...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
ObjectivesThe aim of this study was to investigate the clinical characteristics and the long-term co...
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy withou...
Congenital disorders of cardiac repolarization are associated with risk of serious arrhythmias and s...
The short QT syndrome (SQTS) is a recently described genetic arrhythmogenic disorder, characterized ...
ObjectivesWe aimed to develop diagnostic criteria for the short QT syndrome (SQTS) to facilitate cli...
Short QT syndrome (SQTS) is one of the rarest inheritable cardiac channelopathies, characterized by ...
ObjectivesThis study intends to gain further insights into the natural history, the yield of familia...
The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abno...
Background: Some congenital heart conditions are very rare. In a climate of limited resources, a vie...
Short QT syndrome (SQTS) is an extremely rare inherited arrhythmogenic entity. Nowadays, less than 2...