Galactosemia and Breastfeeding
Babies suffering from galactosemia are unable to process galactose, one of the simple sugars formed by the digestion of breast milk. Galactosemia is a rare inherited disorder that affects about 1 in 60,000 newborns.
Galactosemia and Breastfeeding are an incompatible combination. There may be no initial indication when your child first begins to breastfeed as galactosemia is only detectable through a routine newborn screening process. What happens is that galactose begins to build up to dangerous levels and will eventually damage the liver, central nervous system, eyes, and kidneys.
Even children fed a formula diet are at risk. If your child is diagnosed then your pediatrician will prescribe a special diet to provide the needed nutrition.
Galactosemia is a recessive genetic trait and can be carried by one or both of the parents without either of them showing symptoms. If your family or your partner’s family have a history of galactosemia be sure to let your doctor know immediately.
Even with a positive diagnosis for galactosemia you child will still thrive and grow like any other youngster.
Remember Galactosemia and Breastfeeding are not a compatible combination!
