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Journal of Inherited Metabolic Disease

, Volume 13, Issue 3, pp 263–266 | Cite as

Clinical and biochemical observations on three cases of fructose-1,6-diphosphatase deficiency

  • A. B. Burlina
  • M. Poletto
  • Y. S. Shin
  • F. Zacchello
Short Communication

Keywords

Public Health Internal Medicine Metabolic Disease Biochemical Observation 
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.

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References

  1. Baker, L. and Winegrad, A. I. Fasting hypoglycaemia and metabolic acidosis associated with deficiency of hepatic fructose-1,6-diphosphatase activity.Lancet 2 (1970) 13–16Google Scholar
  2. Dremsek, P. A., Sacher, M., Stogmann, W., Gitzelmann, R. and Bachmann, C. Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test.Eur. J. Pediatr. 144 (1985) 203–204Google Scholar
  3. Elpeleg, O. N., Hurvitz, H., Branski, D. and Barash, V. Fructose-1,6-diphosphatase deficiency: a 20-year follow-up.Am. J. Dis. Child. 143 (1989) 140–141Google Scholar
  4. Krywawych, S., Katz, G., Lawson, A. M., Wyatt, S. and Brenton, D. P. Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiency.J. Inher. Metab. Dis. 9 (1986) 388–392Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1990

Authors and Affiliations

  • A. B. Burlina
    • 1
  • M. Poletto
    • 1
  • Y. S. Shin
    • 2
  • F. Zacchello
    • 1
  1. 1.Department of PaediatricsUniversity of PaduaPaduaItaly
  2. 2.Children's HospitalUniversity of MunichMunich 2FRG

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