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Oxalosis, Type II

Oxalosis, Type II: Introduction

Oxalosis, Type II: 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 the enzyme glyoxylate reductase/hydroxypyruvate reductase. More detailed information about the symptoms, causes, and treatments of Oxalosis, Type II is available below.

Symptoms of Oxalosis, Type II

Home Diagnostic Testing

Home medical testing related to Oxalosis, Type II:

Wrongly Diagnosed with Oxalosis, Type II?

Oxalosis, Type II: Complications

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Causes of Oxalosis, Type II

Read more about causes of Oxalosis, Type II.

Oxalosis, Type II: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Oxalosis, Type II

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 as overactive bladder or...read more »

Oxalosis, Type II: Research Doctors & Specialists

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Oxalosis, Type II: Broader Related Topics

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More information about Oxalosis, Type II

  1. Oxalosis, Type II: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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