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CDG syndrome type 3

CDG syndrome type 3: Introduction

CDG syndrome type 3: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 3 has variable symptoms. More detailed information about the symptoms, causes, and treatments of CDG syndrome type 3 is available below.

Symptoms of CDG syndrome type 3

Wrongly Diagnosed with CDG syndrome type 3?

CDG syndrome type 3: Complications

Review possible medical complications related to CDG syndrome type 3:

Causes of CDG syndrome type 3

Read more about causes of CDG syndrome type 3.

CDG syndrome type 3: Broader Related Topics

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More information about CDG syndrome type 3

  1. CDG syndrome type 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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