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Sialidosis type 1 and 3

Sialidosis type 1 and 3: Introduction

Sialidosis type 1 and 3: A rare inherited biochemical disorder involving the deficiency of an enzyme (alpha-N-acetylneuraminidase) which results in the harmful accumulation of certain chemicals (sialyloligosaccharides and sialylglycopeptides) in various body tissues. More detailed information about the symptoms, causes, and treatments of Sialidosis type 1 and 3 is available below.

Symptoms of Sialidosis type 1 and 3

Sialidosis type 1 and 3: Deaths

Read more about Deaths and Sialidosis type 1 and 3.

Causes of Sialidosis type 1 and 3

Read more about causes of Sialidosis type 1 and 3.

Disease Topics Related To Sialidosis type 1 and 3

Research the causes of these diseases that are similar to, or related to, Sialidosis type 1 and 3:

Sialidosis type 1 and 3: Broader Related Topics

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More information about Sialidosis type 1 and 3

  1. Sialidosis type 1 and 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Deaths
 

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