mayo.edu Congenital long QT syndrome (LQTS) affects an estimated 1 in 2500 people and typically presents with syncope, seizures or sudden death. Whereas someone exhibiting marked prolongation of the ...

Long QT syndrome (LQTS) is the prototypic cardiac ... Towbin JA. Task Force 2: congenital heart disease. J Am Coll Cardiol 2005;45:1326-33. Gregoratos G, Abrams J, Epstein AE, et al.

Protect from light. History of QT prolongation. Congenital long QT syndrome. Recent acute MI. Uncompensated heart failure. Concomitant drugs that cause QT prolongation, including dofetilide ...

Current major projects in the lab focus on the molecular basis of inherited arrhythmia syndromes like catecholaminergic polymorphic ventricular tachycardia (CPVT), congenital long QT syndrome (LQTS), ...

There are cases of sudden cardiac arrest happening among young men and women. According to doctors, most cases happen due to undiagnosed heart conditions like hypertrophic cardiomyopathy, arrhythmias, ...

Congenital LQTS is caused by genetic mutations ... Integrative analysis of KCNQ1 variants reveals molecular mechanisms of ...

Romano-Ward syndrome is a genetic condition associated with a prolonged QT interval on the ECG. Unlike Jervell-Lange-Nielsen, there is no congenital hearing loss present in Romano-Ward syndrome.