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CDG syndrome type 1B

CDG syndrome type 1B: Introduction

CDG syndrome type 1B: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1B has a phosphomannose isomerase enzyme defect. More detailed information about the symptoms, causes, and treatments of CDG syndrome type 1B is available below.

Symptoms of CDG syndrome type 1B

Causes of CDG syndrome type 1B

Read more about causes of CDG syndrome type 1B.

Less Common Symptoms of CDG syndrome type 1B

CDG syndrome type 1B: Broader Related Topics

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More information about CDG syndrome type 1B

  1. CDG syndrome type 1B: Introduction
  2. Symptoms
  3. Causes
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