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

• Psychomotor retardation
• Lipodystrophy
• Brain atrophy
• Skeletal anomalies
• Facial anomalies
• more symptoms...»

See full list of 9 symptoms of CDG syndrome type 3

Wrongly Diagnosed with CDG syndrome type 3?

• Failure to diagnose CDG syndrome type 3
• Undiagnosed: CDG syndrome type 3

CDG syndrome type 3: Complications

Review possible medical complications related to CDG syndrome type 3:

• Premature death (type of Death)
• more complications...»

Causes of CDG syndrome type 3

Read more about causes of CDG syndrome type 3.

CDG syndrome type 3: Broader Related Topics

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

Types of CDG syndrome type 3

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