Glutathionuria
| Glutathionuria | |
|---|---|
| Other names | Gamma-glutamyl transpeptidase deficiency[1] |
 | |
| Glutathione | |
Glutathionuria is the presence of glutathione in the urine, and is a rare inborn error of metabolism.[2]
The condition has been identified in five patients.[3]
References
[edit]- ↑ 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) - ↑ 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.
- ↑ John Fernandes (2006). Inborn metabolic diseases: diagnosis and treatment. Springer. pp. 187–. ISBN 978-3-540-28783-4. Retrieved 1 May 2011.
External links
[edit]
 | This medical sign article is a stub. You can help Wikipedia by adding missing information. |