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520 Possible Causes for Acidosis, Hereditary Fructose Intolerance

  • Hereditary Fructose Intolerance

    [ edit ] a b c d e f "Hereditary fructose intolerance".[] Three aspects of this case expand the published literature on this syndrome: (1) Metabolic acidosis was found to be due to both lactic acidosis and proximal renal tubular[] Abstract Hereditary fructose intolerance is a rare, but potentially lethal, inherited disorder of fructose metabolism, caused by mutation of the aldolase B gene.[]

  • 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[] […] failure and in experimental metabolic acidosis in animals.[] "An experimental renal acidification defect in patients with hereditary fructose intolerance. I. Its resemblance to renal tubular acidosis". J. Clin.[]

  • Fructose-1,6-Diphosphatase Deficiency

    Intravenous fructose tolerance tests provoked severe hypoglycaemia and metabolic acidosis.[] All titles : " Essential fructosuria, hereditary fructose intolerance, and fructose-1,6-diphosphatase deficiency "[] 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[]

  • Acquired Fanconi Syndrome

    Osteomalacia is a rare complication of renal tubular acidosis, and it was reported to be associated with distal renal tubular acidosis in Sjögren’s syndrome.[] Prevention Fanconi's syndrome caused secondarily by the genetic diseases galactosemia, glycogen storage disease, hereditary fructose intolerance, and tyrosinemia is prevented[] The secondary Fanconi syndrome disappears in patients with hereditary fructose intolerance, galactosemia, tyrosinemia, and Wilson disease when these disorders are treated[]

  • Disorder of Fructose Metabolism

    , Fructose, Intolerance, Fructose, hereditary fructose intolerance, Hereditary fructose intolerance syndrome, ALDB - aldolose B deficiency, Fructo-16-bisphosph aldolB def,[] This deficiency compromises gluconeogenesis and results in fasting hypoglycemia, ketosis, and metabolic acidosis. This deficiency can be fatal in neonates.[] Baker L, Winegrad AI (1970) Fasting hypoglycemia and metabolic acidosis associated with deficiency of hepatic fructose-1,6-bisphosphatase activity.[]

  • Renal Tubular Acidosis

    It may be due to metabolic acidosis, usually in children with a hereditary defect in urine acidification.[] Occurs in Fanconi syndrome, which is associated with several genetic diseases (e.g., cystinosis, Wilson disease, tyrosinemia, hereditary fructose intolerance, Lowe syndrome[] […] disease such as Fanconi syndrome , hereditary fructose intolerance, Wilson disease , or oculocerebrorenal syndrome (Lowe syndrome) May also be caused by multiple myeloma[]

  • Glycogen Storage Disease due to Aldolase A Deficiency

    Metabolic Acidosis. ARUP Consult [On-line information]. Available online at . Accessed October 2014. Gaieski, D. et. al. (2013).[] How is Hereditary Fructose Intolerance Diagnosed?[] This deficiency compromises gluconeogenesis and results in fasting hypoglycemia, ketosis, and metabolic acidosis. This deficiency can be fatal in neonates.[]

  • 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[] Dietary changes were introduced gradually until moderate to high levels of ketones appeared in the urine without producing frank metabolic acidosis.[] […] of fructose metabolism E74.10 Disorder of fructose metabolism, unspecified E74.11 Essential fructosuria Inclusion term(s): Fructokinase deficiency E74.12 Hereditary fructose[]

  • Autosomal Dominant Distal Renal Tubular Acidosis

    Fructose Intolerance Hypercalcemia (see Hypercalcemia, [[Hypercalcemia]]) Hyperthyroidism (see Hyperthyroidism, [[Hyperthyroidism]]) Milk Alkali Syndrome (see Milk Alkali[] We searched for SLC4A1 gene mutations in six patients from a Chinese family with a severe phenotype of dRTA (growth impairment, severe metabolic acidosis, with/or without[] fructose intolerance, galactosemia, glycogen storage disease type I, Wilson disease, Lowe syndrome, inherited carbonic anhydrase deficiency) Sporadic Heavy metal poisoning[]

  • Fanconi Renotubular Syndrome 3

    intolerance 1,2 .[] The blood gas analysis was suggestive of a non-anion gap metabolic acidosis with hyperchloremia and hypokalemia.[] Inherited forms mainly present in childhood and may be due to genetic diseases including: galactosaemia, Wilson disease , cystinosis, Lowe syndrome , and hereditary fructose[]

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