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.

G6PD deficiency is very common, and children with G6PD deficiency can still develop normally if properly cared for. However, if not detected and treated promptly, children can suffer from serious sequelae, even cerebral palsy.

G6PD deficiency is a fairly common genetic enzyme disorder in humans. G6PD deficiency can lead to hemolysis, jaundice, yellow eyes and kidney failure. Newborn screening plays an extremely important role in early detection of the disease for active and effective treatment.

Many parents are easily worried when their children have a high fever, especially children with g6pd. The use of fever-reducing drugs for children with g6pd deficiency should be done more carefully with the advice of treating doctors.