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familial polymorphic ventricular tachycardia
Pathology:
- no structural evidence of myocardial disease
Genetics:
- autosomal-dominant
- associated with defects in RYR2
Clinical manifestations:
- relatively early onset
- mortality rate of approximately 30% by the age of 30 years
Special laboratory:
- exercise-stress testing
- salvoes of polymorphic ventricular tachycardias in response to vigorous exercise
General
genetic disease of the heart
polymorphic ventricular tachycardia
Database Correlations
OMIM 192605
References
UniProt :accession Q92736