Table I.
History of SCD |
Family history of premature death |
Causal mutations |
Modifier genes |
History of syncope |
Magnitude of left ventricular hypertrophy |
Extent of myocyte disarray |
Extent of interstitial fibrosis |
Early onset of the disease |
Myocardial ischemia on perfusion tomography |
Abnormal blood pressure response to exercise |
Presence of non-sustained VT on Holter |