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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 
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. 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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