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Up to: Disorder of multiple glycosylation · Congenital disorder of glycosylation type I
Congenital disorder of glycosylation type 1E
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type Ie is characterized by psychomotor delay, seizures, hypotonia, facial dysmorphism and microcephaly. Ocular anomalies are also very common.
This condition has no sub-types.