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Up to: Developmental anomaly of metabolic origin · Disorder of multiple glycosylation · Congenital disorder of glycosylation type II
SLC35A2-congenital disorder of glycosylation
SLC35A2-CDG is a congenital disorder of glycosylation characterized by severe or profound global developmental delay, early epileptic encephalopathy, muscular hypotonia, dysmorphic features (coarse facies, thick eyebrows, broad nasal bridge, thick lips, inverted nipples), variable ocular defects and brain morphological abnormalities on brain MRI (cerebral atrophy, thin corpus callosum).
This condition has no sub-types.