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Sialuria, Finnish type

Sialuria, Finnish type: Introduction

Sialuria, Finnish type: A rare inherited biochemical disorder characterized by the accumulation of sialic acid in the tissues and excretion of sialic acid in the urine. This condition is an adult form of sialuria. More detailed information about the symptoms, causes, and treatments of Sialuria, Finnish type is available below.

Symptoms of Sialuria, Finnish type

Home Diagnostic Testing

Home medical testing related to Sialuria, Finnish type:

Wrongly Diagnosed with Sialuria, Finnish type?

Sialuria, Finnish type: Complications

Read more about complications of Sialuria, Finnish type.

Causes of Sialuria, Finnish type

Read more about causes of Sialuria, Finnish type.

Sialuria, Finnish type: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Sialuria, Finnish type

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Sialuria, Finnish type: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Prognosis for Sialuria, Finnish type

Prognosis for Sialuria, Finnish type: A relatively normal life span can be expected.

Statistics for Sialuria, Finnish type

Sialuria, Finnish type: Broader Related Topics

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Definitions of Sialuria, Finnish type:

Sialuria, Finnish type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Sialuria, Finnish type, or a subtype of Sialuria, Finnish type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Sialuria, Finnish type

  1. Sialuria, Finnish type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis
 

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