Sickle Cell Disease (cont.)IN THIS ARTICLE
What Increases Your RiskRisk of inheriting sickle cell disease Sickle cell disease is an inherited blood disorder, passed from parent to child. Children with sickle cell disease have two defective genes, one from each parent. Various forms of sickle cell disorder occur when a person inherits one sickle cell gene and one other type of defective hemoglobin gene. People who inherit one defective hemoglobin S gene and one normal hemoglobin A gene have sickle cell trait. They don't have symptoms of sickle cell disease nor do their bodies make sickled blood cells. But they have a 50% chance of passing the defective hemoglobin S gene to each of their children.
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, about 2,000 children are born each year with sickle cell disease.2 For more information, see a picture of the risk of passing on an autosomal recessive disease Risk of painful events and complications caused by sickling Triggers that can cause red blood cells to sickle include:
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