Effects of Sickle Cell Disease
Persons with sickle cell disease have abnormally shaped red blood cells. These abnormal cells can cause bone and joint pain, anemia and organ damage. Find out more about sickle cell disease and its symptoms.
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Transcript: Effects of Sickle Cell Disease
What Is Sickle Cell Disease?
Sickle cell disease is a blood disorder that is inherited from both parents. This disorder is more common in certain ethnic groups, such as African Americans, Arabs, Greeks, Italians, Latin and Native Americans.Red Blood Cells in Persons With Sickle Cell Disease
Normal red blood cells are very flexible and are circular in shape, resembling a doughnut. Their flexibility and shape allow them to travel freely through small blood vessels called capillaries. In persons with sickle cell disease, the red blood cells become crescent or sickle-shaped and also become inflexible. The abnormal cells stick inside the capillaries, blocking blood flow to vital organs.Symptoms of Sickle Cell Disease
Persons with sickle cell anemia can have symptoms such as yellow-appearing eyes and skin, pale skin, delayed growth, bone and joint pain, increased risk for infections, development of leg ulcers, eye damage, anemia and damage to the organs affected by the obstruction.Copyrighted animations provided by Blausen Medical.