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669 Possible Causes for Hereditary Fructose Intolerance

  • Hereditary Fructose Intolerance

    […] potentially lethal, inherited disorder of fructose metabolism, caused by mutation of the aldolase B gene.[link.springer.com] How is Hereditary Fructose Intolerance Diagnosed?[dovemed.com] Common Name(s) Hereditary fructose intolerance Hereditary fructose intolerance (HFI) is a metabolic disease caused by the absence of an enzyme called aldolase B.[diseaseinfosearch.org]

  • Oculocerebrorenal Syndrome

    fructose intolerance * The Branchio-Oto-Renal Syndrome * Overproduction type hyperuricemia * Hereditary cystinosis * Hepatorenal tyrosinemia * Renal Disease in Type I Glycogen[acronymfinder.com] […] involvement: monogenic disorders * Nail-patella syndrome * Mitochondrial Diseases of Kidney * Primary Hyperoxaluria * The Oculocerebrorenal Syndrome of Lowe * Fabry's disease * Hereditary[acronymfinder.com]

  • Tyrosinemia Type 1

    Differential diagnosis Differential metabolic diagnoses include classic galactosemia, hereditary fructose intolerance, and fructose 1,6 diphosphatase deficiency, Wilson's[orpha.net] Causes of inherited liver disease include galactosemia, hereditary fructose intolerance, lysosomal storage disease, urea cycle disorders, mitochondrial DNA depletion disorders[clinicaladvisor.com]

  • Dysmyelination with Jaundice

    ., elevated transaminase or hyperbilirubinemia levels) Hemochromatosis (1:300) α 1 -antitrypsin deficiency (1:8,000) Hereditary fructose intolerance (1:20,000 to 1:50,000)[aafp.org] fructose intolerance (1:20,000 to 1:50,000) Glycogen storage diseases (1:25,000) Galactosemia (1:40,000) Organic acidemias (1:50,000) Phospho enol pyruvate carboxykinase[aafp.org] fructose intolerance (1:20,000 to 1:50,000) Mitochondrial disorders (1:30,000; e.g., mitochondrial DNA depletion syndromes) Galactosemia (1:40,000) Wilson's disease (1:50,000[aafp.org]

  • 3Beta-Hydroxy-Delta5-C27-Steroid Oxidoreductase Deficiency

    fructose intolerance) (see these terms), diseases that present with fat and fat soluble vitamin malabsorption, including other liver diseases, and intestinal disease, or[malacards.org] fructose intolerance and a multitude of other conditions.[symptoma.com] fructose intolerance or diseases that present with growth failure (panhypopituitarism) (see these terms).[orpha.net]

  • Hypophosphatemia

    FANCONI SYNDROME Congenital :Cystinosis, Wilson’s disease, hereditary fructose intolerance glycogen storage disease Acquired: Multiple myeloma, SLE, amyloidosis, antiretroviral[slideshare.net]

  • Antimetabolite

    As noted before, a homozygous defect of aldolase B causes hereditary fructose intolerance.[watcut.uwaterloo.ca] […] is promoted by limiting aldolase B activity, heterozygous carriers of a deficient gene for this enzyme experience a greater increase of urate synthesis in response to a fructose[watcut.uwaterloo.ca]

  • Lactulose

    Lactulose should be administrated with caution in infants and small children with autosomal recessive hereditary fructose intolerance.[medicines.org.uk] Patients with rare hereditary problems of galactose or fructose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.[medicines.org.uk] Patients with rare hereditary problems of galactose or fructose intolerance, the Lapp lactase deficiency or glucose-galactose mal-absorption should not take this medicine.[medicines.org.uk]

  • Hyperglobulinemic Purpura

    fructose intolerance (after chronic fructose ingestion) Hyperoxaluria Hyperthyroidism Idiopathic (or hereditary) hypercalciuria Medullary sponge kidney Milk alkali syndrome[clinicclinic2.cafe24.com] fructose intolerance (during fructose ingestion) Lowe's syndrome Metachromatic leukodystrophy Methylmalonic acidemia Monoclonal gammopathy Multiple myeloma Pyruvate carboxylase[clinicclinic2.cafe24.com] Primary biliary cirrhosis Pulmonary fibrosis Sjogren's syndrome Systemic lupus erythematosus Thyroiditis Vasculitis Diseases associated with nephrocalcinosis Fabry's disease Hereditary[clinicclinic2.cafe24.com]

  • Hexokinase Deficiency

    […] is detected in urine If the deficitary enzyme is Aldolase B, the disease that appears is Hereditary Fructose Intolerance , an autosomal recessive disease with a frequency[biochemistryquestions.wordpress.com] For more information about Hereditary Fructose Intolerance : Roths, K.S.: Fructose 1 (P) Aldolase Deficiency (Fructose Intolerance) A good summary about Fructose metabolism[biochemistryquestions.wordpress.com] Since many fruits are rich in fructose, and sucrose and High Fructose Corn Syrup (HFCS) are used for sweeter in the commercial production of many foods, the patient should[biochemistryquestions.wordpress.com]

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