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GENATLAS PHENOTYPE

last update : 09-05-2016

Symbol	CPVT5
Location	6q22.31
Name	catecholaminergic polymorphic ventricular tachycardia 5, with or without muscle weakness
Corresponding gene	TRDN
Main clinical features	arrhythmogenic disorder of the heart characterized by a reproducible form of polymorphic ventricular tachycardia induced by physical activity, stress, or catecholamine infusion, which can deteriorate into ventricular fibrillation recurrent syncope, seizures, or sudden death after physical activity or emotional stress at ECG ventricular arrhythmias of varying morphology not present under resting conditions but appearing only with physical exercise, excitement
Genetic determination	autosomal recessive
Function/system disorder	cardiovascular
Type	disease

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