Hyperoxaluria: Difference between revisions
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Name = Hyperoxaluria | | Name = Hyperoxaluria | |
Revision as of 22:35, 9 June 2010
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Hyperoxaluria | |
DiseasesDB | 31642 |
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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