Glutathionuria

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Glutathionuria
Glutathion.svg
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[edit]

  1. ^ 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. 
  2. ^ John Fernandes (2006). Inborn metabolic diseases: diagnosis and treatment. Springer. pp. 187–. ISBN 978-3-540-28783-4. Retrieved 1 May 2011.