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MeSH Review

Hyperbilirubinemia, Hereditary

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Disease relevance of Hyperbilirubinemia, Hereditary


High impact information on Hyperbilirubinemia, Hereditary


Chemical compound and disease context of Hyperbilirubinemia, Hereditary


Gene context of Hyperbilirubinemia, Hereditary

  • It is concluded that Tc-99m DIPA cholescintigraphy may be helpful in the diagnosis of Rotor syndrome [8].


  1. Erythrocyte membrane transport of glutathione conjugates and oxidized glutathione in the Dubin-Johnson syndrome and in rats with hereditary hyperbilirubinemia. Board, P., Nishida, T., Gatmaitan, Z., Che, M., Arias, I.M. Hepatology (1992) [Pubmed]
  2. Coinheritance of Rotor syndrome, G-6-PD deficiency, and heterozygous beta thalassemia: a possible genetic interaction. Fretzayas, A., Koukoutsakis, P., Moustaki, M., Stavrinadis, C., Karpathios, T. J. Pediatr. Gastroenterol. Nutr. (2001) [Pubmed]
  3. Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemia. Elferink, R.P., Ottenhoff, R., Liefting, W., de Haan, J., Jansen, P.L. J. Clin. Invest. (1989) [Pubmed]
  4. The nicotinic acid test in constitutional conjugated hyperbilirubinemias and effects of corticosteroid. Ohkubo, H., Okuda, K. Hepatology (1984) [Pubmed]
  5. Bilirubin metabolism and the hereditary hyperbilirubinemias. Berk, P.D. Semin. Liver Dis. (1994) [Pubmed]
  6. Bile acid clearance in sheep with hereditary hyperbilirubinemia. Engelking, L.R., Gronwall, R. Am. J. Vet. Res. (1979) [Pubmed]
  7. Biliary excretion of conjugated sulfobromophthalein (BSP) in constitutional conjugated hyperbilirubinemias. Abe, H., Okuda, K. Digestion (1975) [Pubmed]
  8. Cholescintigraphy in the diagnosis of Rotor syndrome. Tutus, A., Silov, G., Kula, M. Clinical nuclear medicine. (1997) [Pubmed]
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