Glutathionuria

Glutathionuria
Other namesGamma-glutamyl transpeptidase deficiency
Glutathione
Frequency0.0001%

Glutathionuria is the presence of glutathione in the urine, and is a rare inborn error of metabolism.

The condition has been identified in five patients.

References

  1. ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Gamma glutamyl transpeptidase deficiency". www.orpha.net. Retrieved 14 April 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ↑ Schulman JD, Goodman SI, Mace JW, Patrick AD, Tietze F, Butler EJ (July 1975). "Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase". Biochem. Biophys. Res. Commun. 65 (1): 68–74. Bibcode:1975BBRC...65...68S. doi:10.1016/S0006-291X(75)80062-3. PMID 238530.
  3. ↑ John Fernandes (2006). Inborn metabolic diseases: diagnosis and treatment. Springer. pp. 187–. ISBN 978-3-540-28783-4. Retrieved 1 May 2011.