Table 3 Outcome of patients versus secondary causes cross-tabulation
From: The outcome of genetic and non-genetic pediatric cardiomyopathies
Alive | Expired | Total | |
|---|---|---|---|
Normal | 102 | 47 | 149 |
VLCAD | 9 | 7 | 16 |
Positive pending | 8 | 16 | 24 |
ELAC2 | 0 | 10 | 10 |
Suspected metabolic disorder | 1 | 7 | 8 |
Douchene muscular dystrophy | 4 | 0 | 4 |
Alstrom syndrome | 4 | 0 | 4 |
Noonan syndrome | 3 | 0 | 3 |
NEXN gene mutation | 3 | 0 | 3 |
Prader–Willi syndrome | 2 | 0 | 2 |
GAA | 0 | 1 | 1 |
Beckwith-Wiedemann syndrome | 1 | 0 | 1 |
Hypochondroplasia | 1 | 0 | 1 |
Connective tissue disorder | 1 | 0 | 1 |
Pompe disease | 1 | 0 | 1 |
SCA | 1 | 0 | 1 |
Total | 141 | 88 | 229 |