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Up to: Cardiogenetic disease · Developmental anomaly of metabolic origin · Disorder of protein N-glycosylation · Congenital disorder of glycosylation type II
MGAT2-congenital disorder of glycosylation
MGAT2-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (large, posteriorly rotated ears with prominent antihelices, convex nasal ridge, open mouth, large and crowded teeth), stereotypic hand movements, seizures, and varying degrees of developmental delay. A bleeding tendency is also observed and this results from diminished platelet aggregation. The disease is caused by loss-of-function mutations in the gene MGAT2 (14q21).
This condition has no sub-types.