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Journal of Inherited Metabolic Disease

, Volume 13, Issue 5, pp 751–752 | Cite as

A new case of argininaemia without spastic diplegia in a Portuguese male

  • L. Vilarinho
  • V. Senra
  • A. Vilarinho
  • C. Barbosa
  • P. Parvy
  • D. Rabier
  • P. Kamoun
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Spastic Diplegia Portuguese Male 
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. Qureshi, I. A., Letarte, J., Ouellet, R., Batshaw, M. L. and Brusilow, S. Treatment of hyperargininemia with sodium benzoate and arginine restricted diet.J. Pediatr. 104 (1984) 473–476Google Scholar
  2. Walser, M. Urea cycle disorders and other hereditary hyperammonemic syndromes. In Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.),The Metabolic Basis of Inherited Disease, 5th edn., McGraw-Hill, New York, 1983, pp. 402–438Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1990

Authors and Affiliations

  • L. Vilarinho
    • 1
  • V. Senra
    • 2
  • A. Vilarinho
    • 2
  • C. Barbosa
    • 2
  • P. Parvy
    • 3
  • D. Rabier
    • 3
  • P. Kamoun
    • 3
  1. 1.Instituto de Genetica MedicaUnidade de Biologia ClinicaPortoPortugal
  2. 2.Hospital Criancas Maria PiaPortoPortugal
  3. 3.Laboratoire de Biochimie Médicale BHôpital Necker-Enfants MaladesParis Cedex 15France

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