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Up to: Syndromic disease · Congenital disorder of glycosylation type II · Defect in conserved oligomeric Golgi complex
COG5-congenital disorder of glycosylation
COG5-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia.
This condition has no sub-types.