Journal of Inherited Metabolic Disease

, Volume 19, Issue 6, pp 793–794 | Cite as

Persistent glycolic aciduria in a healthy child with normal alanine-glyoxylate aminotransferase activity

  • W. J. Craigen
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Healthy Child Aminotransferase Activity 

References

  1. Danpure C, Purdue PE (1995) Primary hyperoxaluria. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic and Molecular Bases of Inherited Disease, 7th edn, New York: McGraw-Hill, 945–961.Google Scholar
  2. Fry DW, Richardson KE (1979a) Isolation and characterization of glycolic acid oxidase from human liver.Biochim Biophys Acta 568: 135–144.Google Scholar
  3. Fry DW, Richardson KE (1979b) Isolation and characterization of glycolic acid dehydrogenase from human liver.Biochim Biophys Acta 567: 482–491.Google Scholar
  4. Jakobs C, Jaeken J, Gibson KM (1993) Inherited disorders of GABA metabolism.J Inher Metab Dis 16: 705–715.Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1996

Authors and Affiliations

  • W. J. Craigen
    • 1
  1. 1.Departments of Molecular and Human Genetics and PediatricsBaylor College of Medicine, One Baylor PlazaHoustonUSA

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