DPM3-congenital disorder of glycosylation

DPM3-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by muscle weakness, waddling gait and dilated cardiomyopathy.

Also known as: CDG syndrome type Io, CDG-Io, CDG1O, DPM3-CDG, DPM3-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type Io, congenital disorder of glycosylation type 1o, congenital disorder of glycosylation type Io

65 clinical trials for this condition and its sub-types.