G6pd deficiency: Glucose-6-phosphate dehydrogenase deficiency is

Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the body. In affected individuals, a defect in an enzyme called glucose-6-phosphate dehydrogenase causes red blood cells to break down prematurely. G6PD deficiency is a hereditary genetic disorder that increases your risk of hemolytic anemia. It happens when your body doesn’t have enough G6PD enzyme. G6PD deficiency is a genetic disorder that affects red blood cells and can cause hemolytic anemia. Learn about the risk factors, triggers, diagnosis, and prevention of this condition from Johns Hopkins Medicine. G6pd deficiency has specific symptoms and causes. Find out about treatment approaches which help control symptoms and support overall well-being.