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1. Congenital muscular dystrophy

2. Danon disease

3. Disorders of fatty acid oxidation

4. Electron transport chain abnormalities

5. Fabry disease

6. Gkycogenosis type III

7. Hemochromatosis

8. D-2-Hydroxyglutaric aciduria

9. 3-Methylglutaconic aciduria II (Barth disease)

10. Mucopolysaccharidosis

11. Pompe disease