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Bookmark or Share- Sickle Cell Disease - Treatment | NHLBI, NIHHydroxyurea is an oral medicine that is frequently prescribed to help treat sickle cell disease. Hydroxyurea is an oral medicine that can reduce sickling of red blood cells and help prevent serious symptoms of sickle cell disease, including pain crises. Healthcare providers usually prescribe daily hydroxyurea for infants as young as 9 months ...
- Sickle Cell Disease - Causes and Risk Factors | NHLBI, NIHThis child has sickle cell trait and is a carrier of the hemoglobin S gene. A 25%, or 1 in 4, chance of inheriting two hemoglobin S genes. This child has sickle cell disease. It is important to keep in mind that each time this couple has a child, the chances of that child having sickle cell disease remain the same.
- Sickle Cell Disease - Diagnosis - NHLBI, NIHNewborn screening programs also find out whether your baby has sickle cell trait and is a carrier of the hemoglobin S gene. If this is the case, genetic counseling will be offered. Remember that when a child has sickle cell trait or sickle cell disease, their future siblings or your child’s future children may be a carrier of the hemoglobin S ...
- Sickle Cell Disease - Sickle Cell Trait - NHLBI, NIHSickle cell trait occurs when a person has one copy of the sickle cell gene passed down from one parent along with a normal hemoglobin gene (hemoglobin A) from the other parent. People who have sickle cell trait are sometimes called carriers . Sickle cell trait is different from sickle cell anemia or sickle cell disease.
- Sickle Cell Disease - What Is Sickle Cell Disease? - NHLBI, NIHSickle cell disease — also called sickle cell anemia — is a group of inherited disorders that affect hemoglobin , the major protein that carries oxygen in red blood cells. Normally, red blood cells are disc-shaped and flexible so they can move easily through the blood vessels.
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