Long QT syndrome is an inherited condition that is characterised by delayed repolarization of the ventricles, which increases the risk of ventricular tachyarrhythmias, leading to syncope, cardiac arrest, or sudden death. It can be diagnosed incidentally on an EKG, following a cardiac event, or the sudden death of a family member. The common variants LQT1 and LQT2 are caused by defects in the alpha subunit of the slow delayed rectifier potassium channel.
A normal corrected QT interval is < 430 ms in men and < 450 ms in women.
Causes of a prolonged QT interval
Classification
Causes
Congenital
Jervell-Lange-Nielsen syndrome (includes deafness due to abnormal potassium channel), Romano-Ward syndrome (no deafness)
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