CDG2h (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 IIh is caused by a defect on chromosome 16q22.1 and involves a defect on the COG8 gene.
See also:
Congenital disorder of glycosylation type IIH:
»Introduction: Congenital disorder of glycosylation type IIH
»Symptoms of Congenital disorder of glycosylation type IIH
CDG2h: Another name for Congenital disorder of glycosylation type IIH (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type IIH
»Symptoms of Congenital disorder of glycosylation type IIH
Some of the symptoms of CDG2h incude:
See full list of 15 symptoms of CDG2h (Congenital disorder of glycosylation type IIH)
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