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

• Liver disease
• Coagulopathy
• Protein-losing enteropathy
• Cyclic vomiting
• Diarrhea
• more symptoms...»

See full list of 8 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

• Unusual facial appearance
• Reduced muscle tone
• Seizures
• more symptoms...»

Read more about symptoms of CDG syndrome type 1B

CDG syndrome type 1B: Broader Related Topics

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions
• more types...»

Types of CDG syndrome type 1B

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