COG1-CDG (CDG-IIg)
Other Names: CDG2G; CDG 2G; Congenital disorder of glycosylation, type IIg ; CDGII/COG1 CEREBROCOSTOMANDIBULAR-LIKE SYNDROME; Congenital disorder of glycosylation type IIg; Congenital disorder of glycosylation type 2G ; CDG syndrome type IIg; Carbohydrate deficient glycoprotein syndrome type IIg; CDG-IIg; COG1-CDG
COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism.
NIH genetic and rare disease info[edit source]
COG1-CDG (CDG-IIg) is a rare disease.
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