Table 2 Secondary cardiomypathy, causes and CMP type
From: The outcome of genetic and non-genetic pediatric cardiomyopathies
Diagnosis CMP Type | |||||
|---|---|---|---|---|---|
Secondary to what? | DCM | HCM | RCM | LVNC | Total |
DCM idiopathic | 84 | 0 | 0 | 0 | 84 |
HCM | 2 | 31 | 1 | 0 | 34 |
Genetic pending results | 21 | 2 | 0 | 0 | 23 |
Post-viral myocarditis | 18 | 0 | 0 | 0 | 18 |
VLCAD | 1 | 14 | 0 | 1 | 16 |
ELAC2 | 2 | 8 | 0 | 0 | 10 |
Suspected metabolic disorder | 8 | 0 | 0 | 0 | 8 |
LV noncompaction | 2 | 0 | 0 | 3 | 5 |
Duchene muscular dystrophy | 4 | 0 | 0 | 0 | 4 |
Alstrom syndrome | 4 | 0 | 0 | 0 | 4 |
Noonan syndrome | 0 | 2 | 0 | 1 | 3 |
RCM | 0 | 0 | 3 | 0 | 3 |
NEXN gene defect | 2 | 0 | 0 | 0 | 2 |
WPW | 2 | 0 | 0 | 0 | 2 |
Prader–Willi Syndrome | 2 | 0 | 0 | 0 | 2 |
Beckwith-Wiedemann syndrome | 0 | 1 | 0 | 0 | 1 |
Chronic kidney disease, nephrotic syndrome | 1 | 0 | 0 | 0 | 1 |
Hypochondroplasia | 1 | 0 | 0 | 0 | 1 |
GAA | 0 | 1 | 0 | 0 | 1 |
Pompe disease | 0 | 1 | 0 | 0 | 1 |
SCA | 1 | 0 | 0 | 0 | 1 |
Sepsis | 1 | 0 | 0 | 0 | 1 |
Suprarenal mass and systemic hypertension | 1 | 0 | 0 | 0 | 1 |
Connective tissue disorder | 1 | 0 | 0 | 0 | 1 |
Vit. D deficiency | 1 | 0 | 0 | 0 | 1 |
Anemia | 1 | 0 | 0 | 0 | 1 |
Autism and DCM M mode 58% | 1 | 0 | 0 | 0 | 1 |
Total | 160 | 60 | 4 | 5 | 229 |