Have a symptom?
See what questions
a doctor would ask.

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

User Interactive Forums

Read about other experiences, ask a question about CDG syndrome type 3, or answer someone else's question, on our message boards:

Related CDG syndrome type 3 Info

Videos about CDG syndrome type 3


More information about CDG syndrome type 3

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

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise