Hereditary Orotic Aciduria and the Excretion of Orotidine

Neuropediatrics. 2016 Dec;47(6):408-409. doi: 10.1055/s-0036-1587594. Epub 2016 Aug 30.

Abstract

Objective Orotic aciduria and deficiency of uridine monophosphate synthetase have been observed in a patient, studied over 10 years, who had no megaloblastic anemia. Excretion of orotic acid and orotidine were 8.24 and 0.52 mmol/mol of creatinine. The ratio of 15.85 differed appreciably from that of 6 patients reported with no megaloblastic anemia. Methods The analysis of orotidine by gas chromotography mass spectrometry was conducted. Conclusion Patients with orotic aciduria with and without megaloblastic anemia cannot be distinguished by ratio of orotic acid to orotidine.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Female
  • Humans
  • Orotate Phosphoribosyltransferase / deficiency*
  • Orotate Phosphoribosyltransferase / drug effects
  • Orotate Phosphoribosyltransferase / urine
  • Orotic Acid / urine*
  • Orotidine-5'-Phosphate Decarboxylase / deficiency*
  • Orotidine-5'-Phosphate Decarboxylase / drug effects
  • Orotidine-5'-Phosphate Decarboxylase / urine
  • Purine-Pyrimidine Metabolism, Inborn Errors / urine*
  • Uridine / analogs & derivatives*
  • Uridine / therapeutic use
  • Uridine / urine
  • Young Adult

Substances

  • Orotic Acid
  • orotidine
  • Orotate Phosphoribosyltransferase
  • Orotidine-5'-Phosphate Decarboxylase
  • Uridine

Supplementary concepts

  • Orotic Aciduria II