Classic galactosemia

Classic galactosemia is a rare genetic disorder where the body cannot properly break down galactose, a sugar found in milk and dairy products. This happens because of a缺乏 an enzyme called galactose-1-phosphate uridyltransferase. Without it, harmful substances build up in the body, leading to symptoms like jaundice, liver damage, swelling, and in severe cases, brain and eye problems. Early diagnosis and a lifelong (dairy-free) diet can help manage the condition and prevent serious complications.