Galactose epimerase deficiency
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Galactose epimerase deficiency, also known as GALE deficiency, Galactosemia III[1] and UDP-galactose-4-epimerase deficiency,[2] is a rare, autosomal recessive form of galactosemia associated with a deficiency of the enzyme galactose epimerase.
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Galactose epimerase deficiency | |
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Other names | Uridine diphosphate galactose-4-epimerase deficiency |
Uridine diphosphate glucose |
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