Haemophagocytosis in hereditary fructose intolerance: a diagnostic dilemma

J Inherit Metab Dis. 1990;13(3):267-9. doi: 10.1007/BF01799369.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acids / urine
  • Blood Coagulation Disorders / etiology
  • Bone Marrow / pathology
  • Diagnosis, Differential
  • Female
  • Fructose / urine
  • Fructose Intolerance / complications
  • Fructose Intolerance / diagnosis*
  • Fructose Intolerance / genetics
  • Glycosuria / urine
  • Histiocytosis, Non-Langerhans-Cell / diagnosis*
  • Histiocytosis, Non-Langerhans-Cell / pathology
  • Humans
  • Infant

Substances

  • Amino Acids
  • Fructose