Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Congenital disorder of glycosylation type I · Disorder of protein N-glycosylation
STT3A-congenital disorder of glycosylation
STT3A-CDG is a form of congenital disorders of N-linked glycosylation characterized by developmental delay, intellectual disability, failure to thrive, hypotonia and seizures. STT3A-CDG is caused by mutations in the gene STT3A (11q23.3).
This condition has no sub-types.