Marked Hyperbilirubinemia-Silent No More!

Am J Med. 2020 Dec;133(12):e733-e734. doi: 10.1016/j.amjmed.2020.04.031. Epub 2020 May 29.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Genetic Predisposition to Disease
  • Gilbert Disease
  • Glucosephosphate Dehydrogenase Deficiency
  • Glucuronosyltransferase / genetics*
  • Homozygote
  • Humans
  • Hyperbilirubinemia / genetics*
  • Male

Substances

  • UGT1A1 enzyme
  • Glucuronosyltransferase