Table 1.
Classification criteria of primary cardiomyopathy according to the American heart association and the European society of cardiology
| Primary cardiomyopathy | ||
|---|---|---|
| Genetic | Mixed* | Acquired |
| • HCM* | • DCM* | • Inflammatory (myocarditis) |
| • ARVC/D* | • Restrictive (nonhypertrophid and nondilated) | • Stress-provoked (*takotsubo) |
| • LV/NC* | • Peripartum | |
| • Glycogen storage (PRKAG2, Danon) | • Tachycardia-induced | |
| • Conduction defects | • Infants of insulin-dependent diabetic mothers | |
| • Mitochondrial myopathies | ||
| • Ion channel Disorders (LQTS, Brugada, SQTS, CVPT, Asian SUNDS) | ||
*HCM: Hypertrophic Cardiomyopathy, *DCM: Dilated Cardiomyopathy, *ARVC/D: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia, *LV/NC: Left Ventricular Noncompaction Cardiomyopathy.