CDGS1A (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
See also:
Congenital disorder of glycosylation type 1A:
»Introduction: Congenital disorder of glycosylation type 1A
»Symptoms of Congenital disorder of glycosylation type 1A
CDGS1A: Another name for Congenital disorder of glycosylation type 1A (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 1A
»Symptoms of Congenital disorder of glycosylation type 1A
Some of the symptoms of CDGS1A incude:
See full list of 58 symptoms of CDGS1A (Congenital disorder of glycosylation type 1A)
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