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Up to: Disorder of multiple glycosylation · Congenital disorder of glycosylation type I
MPDU1-congenital disorder of glycosylation
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type If is characterized by psychomotor delay, seizures, failure to thrive, and cutaneous and ocular anomalies.
This condition has no sub-types.