CDG2g (medical condition): 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 IIg is caused by a defect on chromosome 17q25.1 and involves a defect on the COG1 gene.
See also:
Congenital disorder of glycosylation type 2G:
»Introduction: Congenital disorder of glycosylation type 2G
»Symptoms of Congenital disorder of glycosylation type 2G
CDG2g: Another name for Congenital disorder of glycosylation type 2G (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 2G
»Symptoms of Congenital disorder of glycosylation type 2G
Some of the symptoms of CDG2g incude:
See full list of 8 symptoms of CDG2g (Congenital disorder of glycosylation type 2G)
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