Galactosemia (GAL), due to Gal-1-PO 4 uridyltransferase deficiency, is an inborn error of galactose metabolism causing neonatal morbidity and mortality. The general ...

Looking for reliable medications to treat 'Galactosemia'? This page offers a detailed resource for the most up-to-date treatment options, including both generic and brand-name medications.

Nearly three months after an experimental treatment for classic galactosemia was rejected by the US Food and Drug Administration (FDA), there has been little progress in developing therapies to ...