CDGS2 (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2A has a GlcNAc transferase 2 enzyme defect.
See also:
Congenital disorder of glycosylation type 2A:
»Introduction: Congenital disorder of glycosylation type 2A
»Symptoms of Congenital disorder of glycosylation type 2A
CDGS2: Another name for Congenital disorder of glycosylation type 2A (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 2A
»Symptoms of Congenital disorder of glycosylation type 2A
Some of the symptoms of CDGS2 incude:
See full list of 12 symptoms of CDGS2 (Congenital disorder of glycosylation type 2A)
These medical disease topics may be related to CDGS2:
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