Galactose epimerase deficiency

Galactose epimerase deficiency is a very rare, moderate to severe form of galactosemia characterized by moderate to severe signs of impaired galactose metabolism.

Also known as: GALE deficiency, GALE-D, UDP-galactose-4-epimerase deficiency, epimerase deficiency galactosemia, galactose epimerase deficiency, galactosemia type 3, uridine diphosphate galactose-4-epimerase deficiency, Gale deficiency

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