Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Disorder of multiple glycosylation · Congenital disorder of glycosylation type II
SLC35A1-congenital disorder of glycosylation
SLC35A1-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by repeated hemorrhagic incidents, including severe pulmonary hemorrhage.
This condition has no sub-types.