Hyperoxaluria

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Hyperoxaluria
DiseasesDB 31642
eMedicine med/3027 

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Overview

Hyperoxaluria is an excessive urinary excretion of oxalate. Individuals with hyperoxaluria often have calcium oxalate kidney stones.

Differential Diagnosis of Underlying Causes

Chemicals

Genetic

Autosomal recessive conditions include:

  • Hyperoxaluria, primary type 1
Synonyms include Oxalosis type 1; Oxalosis, primary type 1; Alanine-gloxylate aminotransferase (hepatic) deficiency; Glycolic aciduria
  • Hyperoxaluria, primary type 2
Synonyms include Oxalosis type 2; D-glycerate dehydrogenase deficiency; Glycerate dehydrogenase deficiency; Hydroxypyruvate reductase / glyoxylate reductase deficiency

Idiopathic

Idiopathic hyperoxaluria

Nutritional conditions

  • Malabsorption syndrome
  • Enteric hyperoxaluria

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