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Congenital disorder of glycosylation type 1C: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1C has a ?1,3-glucosyl-transferase enzyme defect. More detailed information about the symptoms, causes, and treatments of Congenital disorder of glycosylation type 1C is available below.
See full list of 13 symptoms of Congenital disorder of glycosylation type 1C
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