Short QT Syndrome (SQTS)

Sponsored diagnostic testing programs for Short QT Syndrome (SQTS)

Short QT Syndrome (SQTS) is a rare inherited cardiac channelopathy marked by an abnormally short QT interval on ECG and a heightened risk of atrial and ventricular arrhythmias. Individuals may experience palpitations, fainting, or sudden cardiac arrest, sometimes without prior warning. Genetic forms often involve pathogenic variants affecting potassium or calcium channels that alter cardiac repolarization.

1 program found for Short QT Syndrome (SQTS)

Programs

1 program
Invitae Unlock™

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers no-charge genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. Eligible patients may access testing at no cost when ordered by a qualified healthcare provider.

Cardiology