38 Possible Causes for Hereditary Fructose Intolerance in USA

    • Hereditary Fructose Intolerance
      Hereditary Fructose Intolerance

      […] contact lab price : contact lab Hereditary Fructose Intolerance Test method(s) : Genotyping (Microarray, Beads, etc.) … Synonym(s) : Fructosemia OMIM Gene Locus Protein ALDOB 9q31.1 Fructose-bisphosphate aldolase B Test TAT : contact lab price : contact lab Hereditary Fructose Intolerance Test … , Bioscientia GmbH - Ingelheim, Germany TAT : contact lab price : contact lab Hereditary Fructose Intolerance Test method(s) : Genotyping (Microarray, Beads, etc.)[1]

    • Gastrointestinal Hemorrhage
      Hereditary Fructose Intolerance
    • Fever
      Hereditary Fructose Intolerance
    • Proximal Renal Tubular Acidosis

      Familial disorders Cystinosis Galactosemia Glycogen storage disease (type I) Hereditary fructose intolerance Lowe syndrome Tyrosinemia Wilson's disease Acquired disorders[2]

    • Fructose

      Intolerance to fructose often only becomes apparent in adulthood and must be distinguished from the rare and potentially dangerous hereditary fructose intolerance (HFI) (See … Hereditary fructose intolerance (HFI) In distinction to the fructose malabsorption described above, HFI is a severe fructose intolerance due to genetic defects (aldolase B … Hereditary fructose intolerance (HFI): about 70% of genetic aberrations (polymorphisms) associated with HFI can currently be identified and these should be determined in case[3]

    • Alitretinoin

      Patients who are allergic to peanut, soya or with rare hereditary fructose intolerance should not take this medicine.[4]

    • Hepatosplenomegaly

      fructose intolerance 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 Hereditaryfructose intolerance • HUS or Hemolytic Uremic Syndrome Treatment for hepatosplenomegaly It should be known that hepatosplenomegaly treatment may be depended on the factor[5] [6]

    • Irinotecan

      Severe myelosuppression may occur Contraindications Hypersensitivity Pregnancy Hereditary fructose intolerance (d/t sorbitol) Cautions Hyperbilirubinemia, elderly, receiving … ., fluconazole, ketoconazole, itraconazole) have hereditary fructose intolerance 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 hereditary fructose intolerance.[7] [8] [9]

    • Fanconi Syndrome

      fructose intolerance. … […] 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 Hereditary Fructose Intolerance Lowe Syndrome Tyrosinemia I Wilson Disease 2.[10] [11]

    • Tyrosinemia Type 1

      Differential diagnosis Differential metabolic diagnoses include classic galactosemia, hereditary fructose intolerance, and fructose 1,6 diphosphatase deficiency, Wilson's[12]

    Hereditary Fructose Intolerance

    Fructose intolerance may refer to fructose malabsorption or hereditary fructose intolerance.

    Further symptoms

    Similar symptoms


    1. GeneTests - Disorders,
    2. Proximal renal tubular acidosis,…
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    4. Alitretinoin,
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    6. Hepatomegaly Brisbane | Glycogen Storage Disease Sydney,
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    8. Campto (irinotecan),…
    9. Irinotecan by Pfizer Canada Inc. - Uses, Side Effects, Interactions,…
    11. Fanconi syndrome,
    12. Orphanet: Tyrosinemia type 1,…