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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