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1. Carnitine transporter deficiency

2. Congenital disorders of glycosylation

3. Farber disease (disseminated lipogranulomatosis)

4. Galactosialidosis

5. Glycogenosis type IV

6. GM1 gangliosidosis

7. Gaucher disease

8. Infantile free sialic acid storage disease (ISSD)

9. Mucolipidosis II-I-cell disease

10. Neonatal hemochromatosis

11. Niemann-Pick disease type C

12. Pearson syndrome (anemia)

13. Siali inverted nipples dosis

14. Sly disease-β-glucuronidase deficiency

15. Wolman disease