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Up to: Congenital disorder of glycosylation type II · Defect in conserved oligomeric Golgi complex
COG4-congenital disorder of glycosylation
COG4-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by seizures, some dysmorphic features, axial hyponia, slight peripheral hypertonia and hyperreflexia.
This condition has no sub-types.