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Oxalosis: A rare inherited metabolic disorder where excess oxalic acid forms crystals which make up urinary stones. In type I primary hyperoxaluria there is a deficiency of peroxisomal alanine-glyoxalate aminotransferase and type II involves a deficiency of the enzyme glyoxylate reductase/hydroxypyruvate reductase. More detailed information about the symptoms, causes, and treatments of Oxalosis is available below.
See full list of 24 symptoms of Oxalosis
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Research the causes of these diseases that are similar to, or related to, Oxalosis:
Commonly undiagnosed diseases in related medical categories:
Interstitial cystitis an under-diagnosed bladder condition: The medical condition of interstitial cystitic is a bladder condition that can be misdiagnosed as various conditions such...read more »
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Choosing the Best Hospital: More general information, not necessarily in relation to Oxalosis, on hospital performance and surgical care quality:
Visit our research pages for current research about Oxalosis treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Oxalosis include:
See full list of 6 Clinical Trials for Oxalosis
Types of Oxalosis
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Excretion of an excessive amount of oxalate in the urine. - (Source - Diseases Database)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Oxalosis as a "rare disease".
Source - Orphanet
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