Glutathionuria
| Glutathionuria | |
|---|---|
 | |
| Glutathione | |
| Classification and external resources | |
| OMIM | 231950 |
Glutathionuria is the presence of glutathione in the urine, and is a rare inborn error of metabolism.[1]
The condition has been identified in five patients.[2]
References
- ↑ 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. 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.
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