What is galactosemia?

Galactosemia is a rare genetic metabolic disorder, in which an individual (usually an infant) lacks the enzyme GALT, which breaks down the sugar galactose in the body. Since (MORE)

What does Galactosemia do?

Galactosemia is an enzyme deficiency that can severely affect newborns. Classic Galactosemia is a rare genetic metabolic disorder. The child with classic galactosemia inher (MORE)