Journal of Inherited Metabolic Disease

, Volume 13, Issue 2, pp 238–238 | Cite as

Non-ketotic hyperglycinaemia: a new case with late onset

  • V. Leuzzi
  • S. Morano
  • F. Moretti
  • F. Fabbrizi
  • I. Antonozzi
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Late Onset 

References

  1. Carson, N. A. J. Non-ketotic hyperglycinaemia — a review of 70 patients.J. Inher. Metab. Dis 5 Suppl. 2 (1982) 126–128Google Scholar
  2. Gerritsen, T., Kaveggia, E. and Waisman, H. A. A new type of idiopathic hyperglycinemia with hypo-oxaluria.Pediatrics 36 (1965) 882–891Google Scholar

Copyright information

© Society for the Study of Inborn Errors of Metabolism and Kluwer Academic Publishers 1990

Authors and Affiliations

  • V. Leuzzi
    • 1
  • S. Morano
    • 1
  • F. Moretti
    • 2
  • F. Fabbrizi
    • 1
  • I. Antonozzi
    • 2
  1. 1.Istituto di Neuropsiatria InfantileRomeItaly
  2. 2.Dipartimento di Medicina Sperimentale Università ‘La Sapienza’RomeItaly

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