Acute hepatic porphyria syndrome with porphobilinogen synthase defect

Int J Biochem. 1980;12(5-6):823-6. doi: 10.1016/0020-711x(80)90170-6.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adult
  • Amino Acids / metabolism
  • Aminolevulinic Acid / urine
  • Erythrocytes / metabolism
  • Feces / analysis
  • Female
  • Humans
  • Lead / metabolism
  • Liver Diseases / enzymology*
  • Male
  • Porphobilinogen / urine
  • Porphobilinogen Synthase / genetics
  • Porphobilinogen Synthase / metabolism*
  • Porphyrias / enzymology*
  • Porphyrias / genetics
  • Porphyrins / metabolism
  • Syndrome

Substances

  • Amino Acids
  • Porphyrins
  • Lead
  • Porphobilinogen
  • Aminolevulinic Acid
  • Porphobilinogen Synthase