A rare, genetic, cardiac rhythm disease characterized by ventricular fibrillation in the absence of any structural or functional heart disease, or known repolarization abnormalities. The presence of J waves is associated with a higher risk of nocturnal ventricular fibrillation events and a higher risk of recurrence.
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short QT syndrome
MONDO:0000453
ventricular tachycardia, familial
MONDO:0008648
ventricular fibrillation, paroxysmal familial, type 1
MONDO:0011376
familial sick sinus syndrome
MONDO:0012061
ventricular fibrillation, paroxysmal familial, 2
MONDO:0013063
atrial conduction disease
MONDO:0014500