Sickle Cell Disease
Sickle cell disease (also known as sickle cell anemia) is a genetic blood disorder characterized by red blood cells with an abnormal, crescent-like shape. It affects the body’s ability to make use of oxygen, and can cause extreme pain, organ damage, and an increased risk of infection and stroke. Sickle cell disease affects millions of people worldwide, particularly those of African descent. Treatment consists of medications, blood transfusions, and nutritional support. Early diagnosis is key to managing the disease since it can lead to a lower chance of complications and increased quality of life.
← International Journal of Blood Transfusion