Galactosemia is a genetic condition that prevents the breakdown of galactose, found in dairy products. Symptoms include a distended stomach, jaundice, slow growth, and eye, liver, kidney, and brain damage. Blood tests can diagnose the condition, and if left untreated, it can cause intellectual difficulties and eye damage. Galactosemia is a medical condition resulting from […]
Galactosemia is a rare genetic disease that prevents the body from breaking down galactose, a type of sugar found in dairy products. Infants with this disorder require a specialized formula, usually soy-based or Nutramigen, a specially developed type of protein. Parents should consult their pediatricians and watch their baby closely during the first few weeks […]
