Hyperoxaluria

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

• Ethylene glycol
• Oxalate poisoning
• Cellulose sodium phosphate

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