Add to ORKGLong QT syndrome (LQTS) is an inherited ion channelopathy resulting in abnormal ventricular repolarization and abnormal prolongation of QT interval on the ECG. Syncope, fainting, cardiac arrest, and sudden death are common manifestations of LQTS. We present a case report that describes a patient with prolonged QT interval after extrasystoles and a family history of sudden cardiac death
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
Introduction: Long QT syndrome (LQTS) is an uncommon disorder that can lead to potentially life-thre...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...
Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on EC...
Background—A prolonged QT interval is associated with a risk for life-threatening events. However, l...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
The long QT syndrome (LQTS) is an arrhythmogenic syndrome due to cardiac ion channel disorders chara...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Syncope is a common presentation to emergency departments. Arrhythmias account for 14% of those pres...
The QT interval duration is greater than 50% of the RR interval, a good indication that it is prolon...
We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT ...
The congenital long QT syndrome (LQTS) is characterized by abnormally prolonged ventricular repolari...
Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia,...
A large number of studies has been carried out to investigate the pathophysiology and the clinical i...
A 71-year-old woman collapsed while working as a grocery store cashier. CPR was performed and an AED...
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
Introduction: Long QT syndrome (LQTS) is an uncommon disorder that can lead to potentially life-thre...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...
Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on EC...
Background—A prolonged QT interval is associated with a risk for life-threatening events. However, l...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
The long QT syndrome (LQTS) is an arrhythmogenic syndrome due to cardiac ion channel disorders chara...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Syncope is a common presentation to emergency departments. Arrhythmias account for 14% of those pres...
The QT interval duration is greater than 50% of the RR interval, a good indication that it is prolon...
We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT ...
The congenital long QT syndrome (LQTS) is characterized by abnormally prolonged ventricular repolari...
Acquired long QT syndrome is typically caused by medications, electrolyte disturbances, bradycardia,...
A large number of studies has been carried out to investigate the pathophysiology and the clinical i...
A 71-year-old woman collapsed while working as a grocery store cashier. CPR was performed and an AED...
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
Introduction: Long QT syndrome (LQTS) is an uncommon disorder that can lead to potentially life-thre...
Long QT syndrome (LQTS) is an arrhythmogenic cardio-vascular disorder resulting from mutations in ca...