PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0013264|duchenne muscular dystrophy |
| Sentences | 1 |
| PubMedID- 22761912 | The blood creatin phosphokinase enzyme and urine glycerol were normal in all cases, indicating that there was no contiguous deletion syndrome with duchenne muscular dystrophy or glycerol kinase deficiency. |
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