Sickle cell disease is an inherited disorder. More
specifically, sickle cell disease is an
autosomal recessive disease. This means that to have
the disease, a person must inherit an abnormal gene from both parents.
People whose ancestors were from Africa, India, the Middle East, the
Mediterranean (Turkey, Italy, Greece), and some Latin American countries are
more likely to inherit the gene that can cause sickle cell disease. In the
United States, the disease mainly affects African-Americans (1 in 650) and
Latin Americans (1 in 1,000 to 1,400).1 Of
African-Americans, 8% carry the
sickle cell trait.2
Some people inherit one sickle cell gene and one defective hemoglobin
gene of another type. This results in similar sickle cell disorders ranging
from mild to severe. As a group, these disorders occur as frequently as does
sickle cell anemia in the U.S.