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Journal of Inherited Metabolic Disease

, Volume 15, Issue 6, pp 937–938 | Cite as

5-Oxoprolinuria due to glutathione synthetase deficiency

  • R. Kumar Pejaver
  • A. H. Watson
Case Report

Keywords

Public Health Internal Medicine Glutathione Metabolic Disease Glutathione Synthetase 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Meister A (1974) The γ-glutamyl cycle and diseases associated with specific enzymatic deficiencies.Ann Intern Med 81: 247.Google Scholar
  2. Meister A, Larsson A (1989) Glutathione synthase deficiency and other disorders of the γ-glutamyl cycle. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 855–868.Google Scholar
  3. Speilberg SP, Boxer LA, Corash LM, Schulman JD (1979) Improved erythrocyte survival with high dose vitamin E in chronic hemolysing G6PD and glutathione synthetase deficiency.Ann Intern Med 90: 53–54.Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1992

Authors and Affiliations

  • R. Kumar Pejaver
    • 1
  • A. H. Watson
    • 1
  1. 1.Department of PaediatricsSt Mary's HospitalNewportUK

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