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Neuraminidase deficiency, type II, juvenile form

Neuraminidase deficiency, type II, juvenile form: Introduction

Neuraminidase deficiency, type II, juvenile form: A rare inherited disorder involving an enzyme (neuraminidase and beta-galactosidase) deficiency which results in a build up of glycoproteins (sialyloligosaccharides) in the urine. The juvenile form of the condition is less severe than the infantile form which causes death within months of birth. More detailed information about the symptoms, causes, and treatments of Neuraminidase deficiency, type II, juvenile form is available below.

Symptoms of Neuraminidase deficiency, type II, juvenile form

Home Diagnostic Testing

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Causes of Neuraminidase deficiency, type II, juvenile form

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Disease Topics Related To Neuraminidase deficiency, type II, juvenile form

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Neuraminidase deficiency, type II, juvenile form: Undiagnosed Conditions

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Misdiagnosis and Neuraminidase deficiency, type II, juvenile form

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Neuraminidase deficiency, type II, juvenile form: Research Doctors & Specialists

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More information about Neuraminidase deficiency, type II, juvenile form

  1. Neuraminidase deficiency, type II, juvenile form: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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