Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome

Pediatr Int. 2007 Aug;49(4):540-2. doi: 10.1111/j.1442-200X.2007.02410.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Female
  • Gilbert Disease / complications*
  • Gilbert Disease / genetics
  • Glucuronosyltransferase / genetics
  • Humans
  • Hyperbilirubinemia / complications*
  • Mutation
  • Spherocytosis, Hereditary / complications*

Substances

  • Glucuronosyltransferase