A rare genetic condition, galactosemia results in the inability to breakdown galactose into glucose. The breakdown cannot occur due to the absence of a specific enzyme.
Understand that infants in the United States are routinely screened for galactosemia shortly after birth. Ask your doctor if your newborn has been screened for the disorder, or request that a screening be performed. The quality of life in i… Source:http://www.ehow.com/how_2047869_treat-galactosemia.html