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.

Also known as: CDG syndrome type If, CDG-If, CDG1F, CDGIf, MPDU1-CDG, carbohydrate deficient glycoprotein syndrome type If, congenital disorder of glycosylation type 1f, congenital disorder of glycosylation type If

0 clinical trials for this condition and its sub-types, 0 tagged with MPDU1-congenital disorder of glycosylation itself.