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Sickle Cell Anemia & African Americans
What's Inside
Sickle Cell - Sickle cell anemia occurs in about one in 600 African American births. Learn about the signs, symptoms, diagnosis and treatments.
   Common and Severe Complication of Sickle Cell Disease
   NATURAL REMEDIES FOR SICKLE CELL
   Sickle Cell
   Sickle Cell Complication
   What Do We Know About Heredity and Sickle Cell Disease?
Ryan Clark: Pro-Athlete Without A Spleen

(BlackDoctor.org) -- One might wonder how hard it would be for the average man to return to a regular-life routine after having his spleen and gallbladder removed. But what about an NFL player? What about a person whose job depends greatly on his overall state of health?

Ryan Clark, safety for the Pittsburgh Steelers, was rushed to the hospital after a football game in Denver in 2007 due to complications from sickle cell trait. In the Denver altitude, portions of Clark’s spleen lost

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The Facts About Sickle Cell Disease

(BlackDoctor.org) -- Did you know that approximately 1 in 12 African Americans carry the sickle cell trait? Each year, about 1 in 500 African Americans is born with sickle cell disease.

Sickle cell disease is an inherited blood disorder that affects red blood cells. People with sickle cell disease have red blood cells that contain mostly hemoglobin* S, an abnormal type of hemoglobin. Sometimes these red blood cells become sickle-shaped (crescent shaped) and have difficulty passing

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Working Toward A Cure For Sickle Cell Anemia

(BlackDoctor.org) -- Scientists in the U.S. have made a breakthrough in the fight against sickle cell anemia, a blood disease caused by a defect in a single gene.

Sickle cell anemia is a serious condition in which the red blood cells can become sickle-shaped instead of smooth and round. They do not move easily through the blood because they are stiff and sticky and can form clumps in the blood vessels.

These clumps block the blood flow in blood vessels and can cause pain, serious

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Early Sickle Cell Complications Don't Predict Later Risk

(BlackDoctor.org)-- A study conducted by scientists at the University of Texas Southwestern Medical Center at Dallas concluded that infants and toddlers with sickle cell disease who have pain episodes or dactylitis —painful swelling in the feet and hands —are not at increased risk of suffering those symptoms again later in childhood.

However, young children with the disease who are hospitalized for chest problems are more likely to have a recurrence of those problems up to adulthood,

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