Congenital disorders of glyscosylation (CDG) are a group of rare metabolic disorders that result from mutations in genes involved in the glycosylation of proteins and lipids. Patients typically display multi-system defects that can include developmental delay, failure to thrive, seizures, cognitive impairment, endocrine defects, and coagulation abnormalities.
Below we list only some of the known CDG subtypes and their causative genes. Please see the general information links or search OMIM for "congenital disorders of glycosylation" to see more types.
General information links for Congenital disorders of glyscosylation: