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

J Inherit Metab Dis. 1990;13(3):263-6. doi: 10.1007/BF01799368.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Acidosis, Lactic / etiology
  • Child, Preschool
  • Fructose-1,6-Diphosphatase Deficiency / complications
  • Fructose-1,6-Diphosphatase Deficiency / diet therapy
  • Fructose-1,6-Diphosphatase Deficiency / physiopathology*
  • Glycerol / urine
  • Humans
  • Hypoglycemia / etiology
  • Infant
  • Infant, Newborn
  • Male
  • Uric Acid / blood

Substances

  • Uric Acid
  • Glycerol