Brandon Cooke

Methods Chart review identified children and young people with LQT1 and LQT2 using the inherited cardiac conditions database at the Royal Belfast Hospital for Sick Children and electronic patient records, yielding a total of 152 patients.

Introduction Congenital long QT syndrome is a genetic condition causing delayed myocardial repolarisation, resulting in a prolonged QTc segment on a resting electrocardiography, which is associated with ventricular arrhythmia and sudden cardiac death.