Intolerance to fructose often only becomes apparent in adulthood and must be distinguished from the rare and potentially dangerous hereditaryfructoseintolerance (HFI) (See … Hereditaryfructoseintolerance (HFI) In distinction to the fructose malabsorption described above, HFI is a severe fructose intolerance due to genetic defects (aldolase B … Hereditaryfructoseintolerance (HFI): about 70% of genetic aberrations (polymorphisms) associated with HFI can currently be identified and these should be determined in case
fructoseintolerance Glycogen storage disease Primary biliary cirrhosis Sarcoidosis Sclerosing cholangitis Haemolytic-uremic syndrome (HUS) Reye's syndrome Diagnosis Your … Alcohol Hepatitis A Hepatitis B Congestive heart failure Infectious mononucleosis Leukemia Tumour metastases Neuroblastoma Hepatocellular carcinoma Niemann-Pick disease Hereditary … fructoseintolerance • HUS or Hemolytic Uremic Syndrome Treatment for hepatosplenomegaly It should be known that hepatosplenomegaly treatment may be depended on the factor
Severe myelosuppression may occur Contraindications Hypersensitivity Pregnancy Hereditaryfructoseintolerance (d/t sorbitol) Cautions Hyperbilirubinemia, elderly, receiving … ., fluconazole, ketoconazole, itraconazole) have hereditaryfructoseintolerance have taken ketoconazole within the past week What side effects are possible with this medication … Campto infusion contains sorbitol and may be unsuitable for people with hereditaryfructoseintolerance.
fructoseintolerance. … […] recognised causes are Wilson's disease (a genetically inherited condition of copper metabolism), Lowe syndrome, tyrosinemia (type I), galactosemia, glycogen storage diseases, and hereditary … Inborn Errors of Metabolism Cystinosis Galactosemia I & III Glycogenosis - GSD Ia & XI HereditaryFructoseIntolerance Lowe Syndrome Tyrosinemia I Wilson Disease 2.