G6PD deficiency is a common genetic disease in which red blood cells break down and do not function normally. Newborns with this condition often have severe anemia, jaundice, and are prone to later cerebral palsy.

Newborn screening programs aim to detect metabolic disorders in children early, helping to prevent dangerous complications and giving children a normal, healthy life.

G6PD deficiency is a fairly common metabolic disorder. For children with G6PD deficiency, parents need to develop a scientific nutritional regimen to help their children have a healthy life. So what should parents pay attention to when using food for children with G6PD deficiency?

People with thalassemia can still have a normal life, get married, and have children like everyone else. However, they must adhere to lifelong treatment by continuous blood transfusions and iron excretion.