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830 Possible Causes for Hereditary Fructose Intolerance, Neuronal Loss and Gliosis in the Inferior Olives

  • Disorder of Fructose Metabolism

    , Fructose, Intolerance, Fructose, hereditary fructose intolerance, Hereditary fructose intolerance syndrome, ALDB - aldolose B deficiency, Fructo-16-bisphosph aldolB def,[fpnotebook.com] There was marked depletion of cerebellar Purkinje cells, with sparing of the granular layer and neuronal loss in the dentate nuclei and inferior olives.[clinicalgate.com] Other "What Is Hereditary Fructose Intolerance?"[medical-dictionary.thefreedictionary.com]

  • Hereditary Fructose Intolerance

    [ edit ] a b c d e f "Hereditary fructose intolerance".[en.wikipedia.org] Abstract Hereditary fructose intolerance is a rare, but potentially lethal, inherited disorder of fructose metabolism, caused by mutation of the aldolase B gene.[ncbi.nlm.nih.gov] As mentioned, a complete lack of tooth decay can also serve as an indicator for hereditary fructose intolerance.[symptoma.com]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Hypoglycemia

    Congenital enzyme deficiencies include hereditary fructose intolerance, galactosemia, and leucine sensitivity of childhood.[emedicine.com] 1,6 diphosphatase deficiency; phosphoenolpyruvate deficiency; pyruvate carboxylase deficiency; galactosemia; hereditary fructose intolerance; and maple syrup urine disease[emedicine.com] In hereditary fructose intolerance and galactosemia, an inherited deficiency of a hepatic enzyme causes acute inhibition of hepatic glucose output when fructose or galactose[emedicine.com]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Fructose-1,6-Diphosphatase Deficiency

    All titles : " Essential fructosuria, hereditary fructose intolerance, and fructose-1,6-diphosphatase deficiency "[agris.fao.org] 2014 ICD-9-CM Diagnosis Code 271.2 Hereditary fructose intolerance 2014 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 Short description: Hered fructose intoleran[icd9data.com] Functional and molecular modelling studies of two hereditary fructose intolerance-causing mutations at arginine 303 in human liver aldolase.[emedicine.com]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Congenital Bile Acid Synthesis Defect Type 2

    fructose intolerance or diseases that present with growth failure (panhypopituitarism) (see these terms).[orpha.net] […] which includes alpha-1-antitrypsin deficiency (ZZ phenotype), tyrosinemia type 1, biliary atresia, choledochal cyst, cystic fibrosis, Alagille syndrome, galactosemia and hereditary[orpha.net]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Proximal Renal Tubular Acidosis

    In three unrelated patients with hereditary fructose intolerance (HFI), but in none of five normal subjects, the experimental administration of fructose invariably induced[doi.org] fructose intolerance Lowe syndrome Tyrosinemia Wilson's diseaseAcquired disorders Amyloidosis Multiple myeloma Paroxysmal nocturnal hemoglobinuria Toxins, such as HAART,[en.wikipedia.org] "An experimental renal acidification defect in patients with hereditary fructose intolerance. I. Its resemblance to renal tubular acidosis". J. Clin.[ipfs.io]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Congenital Bile Acid Synthesis Defect Type 4

    fructose intolerance or diseases that present with growth failure (panhypopituitarism) (see these terms).[orpha.net] […] which includes alpha-1-antitrypsin deficiency (ZZ phenotype), tyrosinemia type 1, biliary atresia, choledochal cyst, cystic fibrosis, Alagille syndrome, galactosemia and hereditary[orpha.net]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Sucrose Intolerance

    Hereditary fructose intolerance is inherited, which means it can be passed down through families.[medlineplus.gov] , Galactosemia, Hereditary Fructose Intolerance & Sorbitol Diabetic Cataracts PKU, Phenylketonuria, Galactosemia, Hereditary Fructose Intolerance & Sorbitol Diabetic Cataracts[skvid.me] Individuals who are obligate heterozygotes do not demonstrate the symptoms of hereditary fructose intolerance (HFI).[reference.medscape.com]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Disorder of Carbohydrate Metabolism

    Metabolism Hereditary Fructose Intolerance -Hereditary fructose intolerance is due to a deficiency of fructose-1-phosphate aldolase B which converts fructose into two 3-carbon[slideplayer.com] […] of fructose metabolism E74.10 Disorder of fructose metabolism, unspecified E74.11 Essential fructosuria Inclusion term(s): Fructokinase deficiency E74.12 Hereditary fructose[icd10coded.com] Hereditary fructose intolerance Hereditary fructose intolerance is caused by mutation in the gene encoding Aldolase B enzyme.[namrata.co]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives
  • Renal Tubular Acidosis

    Occurs in Fanconi syndrome, which is associated with several genetic diseases (e.g., cystinosis, Wilson disease, tyrosinemia, hereditary fructose intolerance, Lowe syndrome[unboundmedicine.com] […] disease such as Fanconi syndrome , hereditary fructose intolerance, Wilson disease , or oculocerebrorenal syndrome (Lowe syndrome) May also be caused by multiple myeloma[merckmanuals.com] fructose intolerance, galactosemia, glycogen storage disease type I, Wilson disease, Lowe syndrome, inherited carbonic anhydrase deficiency) Sporadic Heavy metal poisoning[unboundmedicine.com]

    Missing: Neuronal Loss and Gliosis in the Inferior Olives

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