Add to ORKGLong QT syndrome is one of the most feared entities in hospitalized patients due to the potential risk for ventricular tachycardia and sudden death. Association between channelopathies and congenital cardiomyopathy is a new entity that has been studied recently. We report an interesting case of this association that maybe related to a genetic mutation
We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillat...
Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia,...
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and su...
Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarizat...
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation o...
The hereditary long QT syndrome (LQTS) is a genetic channelopathy with variable penetrance that is a...
Forty per cent (40%) of sudden unexpected natural deaths in people under 35 years of age are associa...
BACKGROUND: Although QT prolongation following myocardial infarction (MI) is generally moderate, cas...
This article presents the case of a 35 year-old male with long QT syndrome (LQTS) who suffered from ...
AbstractIt is becoming clear that mutations in the KVLQT1, human “ether-a-go-go” related gene, cardi...
Background: Left ventricular non-compaction (LVNC) is an abnormality of the myocardium, characterize...
The congenital long QT syndrome (LQTS) is characterized by abnormally prolonged ventricular repolari...
Long QT syndrome (LQTS) is characterized by abnormal prolongation of the QT interval on the surface ...
Congenital long-QT syndrome (LQTS) and Brugada syndrome (BrS) are cardiac channelopathies caused by ...
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy withou...
We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillat...
Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia,...
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and su...
Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarizat...
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation o...
The hereditary long QT syndrome (LQTS) is a genetic channelopathy with variable penetrance that is a...
Forty per cent (40%) of sudden unexpected natural deaths in people under 35 years of age are associa...
BACKGROUND: Although QT prolongation following myocardial infarction (MI) is generally moderate, cas...
This article presents the case of a 35 year-old male with long QT syndrome (LQTS) who suffered from ...
AbstractIt is becoming clear that mutations in the KVLQT1, human “ether-a-go-go” related gene, cardi...
Background: Left ventricular non-compaction (LVNC) is an abnormality of the myocardium, characterize...
The congenital long QT syndrome (LQTS) is characterized by abnormally prolonged ventricular repolari...
Long QT syndrome (LQTS) is characterized by abnormal prolongation of the QT interval on the surface ...
Congenital long-QT syndrome (LQTS) and Brugada syndrome (BrS) are cardiac channelopathies caused by ...
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy withou...
We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillat...
Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia,...
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and su...