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CDG syndrome type 1A

CDG syndrome type 1A: Introduction

CDG syndrome type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function. More detailed information about the symptoms, causes, and treatments of CDG syndrome type 1A is available below.

Symptoms of CDG syndrome type 1A

Wrongly Diagnosed with CDG syndrome type 1A?

CDG syndrome type 1A: Complications

Review possible medical complications related to CDG syndrome type 1A:

Causes of CDG syndrome type 1A

Read more about causes of CDG syndrome type 1A.

CDG syndrome type 1A: Broader Related Topics

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More information about CDG syndrome type 1A

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

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