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Table 6 Metabolic disease as causes of conjugated hyperbilirubinemia in infancy

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 %

  1. *See text for complete list and count of “unknown” diagnoses