Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity

Am J Med. 1969 Sep;47(3):395-409. doi: 10.1016/0002-9343(69)90224-1.
No abstract available

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Bile / chemistry
  • Bile Pigments / analysis
  • Bilirubin / analysis
  • Bilirubin / blood
  • Bilirubin / metabolism
  • Child, Preschool
  • Female
  • Genes, Dominant
  • Genotype
  • Glucuronates / metabolism*
  • Glucuronates / urine
  • Humans
  • Hyperbilirubinemia, Hereditary / complications*
  • Hyperbilirubinemia, Hereditary / genetics
  • Jaundice / complications
  • Jaundice / drug therapy
  • Liver / enzymology
  • Male
  • Metabolism, Inborn Errors / complications*
  • Metabolism, Inborn Errors / genetics
  • Pedigree
  • Phenobarbital / pharmacology
  • Phenobarbital / therapeutic use
  • Phenotype
  • Transferases / metabolism*

Substances

  • Bile Pigments
  • Glucuronates
  • Transferases
  • Bilirubin
  • Phenobarbital