CDG2f (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 IIf is caused by a defect on chromosome 6q25.16q15 and involves a defect on the gene for CMP-sialic acid transporter.
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Congenital disorder of glycosylation type 2F:
»Introduction: Congenital disorder of glycosylation type 2F
»Symptoms of Congenital disorder of glycosylation type 2F
CDG2f: Another name for Congenital disorder of glycosylation type 2F (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 2F
»Symptoms of Congenital disorder of glycosylation type 2F
Some of the symptoms of CDG2f incude:
Read more about symptoms of CDG2f (Congenital disorder of glycosylation type 2F)
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