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Neuraminidase deficiency

Neuraminidase deficiency: Introduction

Neuraminidase deficiency: A rare inherited disorder involving an enzyme (neuraminidase and beta-galactosidase) deficiency which results in a build up of glycoproteins (sialyloligosaccharides) in the urine. More detailed information about the symptoms, causes, and treatments of Neuraminidase deficiency is available below.

Symptoms of Neuraminidase deficiency

Home Diagnostic Testing

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Wrongly Diagnosed with Neuraminidase deficiency?

Causes of Neuraminidase deficiency

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Disease Topics Related To Neuraminidase deficiency

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Neuraminidase deficiency: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Neuraminidase deficiency

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Neuraminidase deficiency: Research Doctors & Specialists

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Evidence Based Medicine Research for Neuraminidase deficiency

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Research about Neuraminidase deficiency

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Statistics for Neuraminidase deficiency

Neuraminidase deficiency: Broader Related Topics

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Definitions of Neuraminidase deficiency:

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Neuraminidase deficiency as a "rare disease".
Source - Orphanet

Related Neuraminidase deficiency Info

Videos about Neuraminidase deficiency

 

More information about Neuraminidase deficiency

  1. Neuraminidase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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