See what questions
a doctor would ask.
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.
Review possible medical complications related to CDG syndrome type 3:
Read more about causes of CDG syndrome type 3.
Read about other experiences, ask a question about CDG syndrome type 3, or answer someone else's question, on our message boards:
Search Specialists by State and City