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Up to: Congenital disorder of glycosylation type II · Defect in conserved oligomeric Golgi complex
COG8-congenital disorder of glycosylation
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIh is characterized by severe psychomotor retardation, failure to thrive and intolerance to wheat and dairy products.
This condition has no sub-types.