Short QT syndrome

A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified

Also known as: short QT syndrome, ventricular arrhythmia associated with short QT syndrome, familial short QT syndrome

33 clinical trials for this condition and its sub-types, 1 tagged with Short QT syndrome itself.