Journal of Inherited Metabolic Disease

, Volume 16, Issue 6, pp 1054–1056 | Cite as

Arginase deficiency in two brothers

  • M. Candito
  • B. Bebin
  • C. Vianey-Saban
  • D. Rabier
  • S. Bekri
  • F. Sebag
  • P. Chambon
  • P. Kamoun
Case Report

Keywords

Public Health Internal Medicine Arginase Arginase Deficiency 

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References

  1. Brusilow SW, Horwich AL (1989) Urea cycle enzymes. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease. New York: McGraw Hill, 629–663.Google Scholar
  2. Cederbaum SD, Moedjono SJ, Shaw KNF, Carter M, Naylor E, Walser M (1982) Treatment of hyperargininaemia due to arginase deficiency with a chemically defined diet.J Inher Metab Dis 5: 95–99.Google Scholar
  3. Marescau B, De Deyn PP, Lowenthal A et al (1990) Guanidino compound analysis as a complementary diagnostic parameter for hyperargininaemia: follow-up of guanidino compound levels during therapy.Pediatr Res 27: 297–303.Google Scholar

Copyright information

© Society for the Study of Inborn Errors of Metabolism and Kluwer Academic Publishers 1993

Authors and Affiliations

  • M. Candito
    • 1
  • B. Bebin
    • 2
  • C. Vianey-Saban
    • 3
  • D. Rabier
    • 4
  • S. Bekri
    • 1
  • F. Sebag
    • 1
  • P. Chambon
    • 1
  • P. Kamoun
    • 4
  1. 1.Laboratoire de BiochimieHôpital PasteurNice Cedex 1France
  2. 2.Service de PédiatrieHôpital des BroussaillesCannesFrance
  3. 3.Laboratoire de BiochimieHôpital DebrousseLyon Cedex 05France
  4. 4.Laboratoire de Biochimie Médicale BHôpital Necker-Enfants MaladesParis Cedex 15France

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