From: Etiologies of conjugated hyperbilirubinemia in infancy: a systematic review of 1692 subjects
Total number | % of total | |
---|---|---|
Galactosemia | 27 | 36.49 % |
Glycogen Storage Disease | 7 | 9.46 % |
Tyrosinemia | 6 | 8.11 % |
Iron Storage Disease | 6 | 8.11 % |
Niemann-Pick | 4 | 5.41 % |
Zellweger | 3 | 4.05 % |
Fat storage disease | 2 | 2.70 % |
Hereditary fructose intolerance | 2 | 2.70 % |
HMG CoA lyase deficiency | 1 | 1.35 % |
Citrullinemia | 1 | 1.35 % |
Methyl-malonic acidemia | 1 | 1.35 % |
Gaucher disease | 1 | 1.35 % |
Unknown* | 13 | 17.57 % |
Total | 74 | 100.00 % |