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Bookmark or Share- Sickle Cell Disease - What Is Sickle Cell Disease? | NHLBI, NIHLast updated on April 22, 2024. Back to top. Sickle cell disease is an inherited blood disorder that affects hemoglobin, the protein that carries oxygen through the body. Misshapen red blood cells can block blood flow causing lifelong health problems.
- Sickle cell anemia - Diagnosis & treatment - Mayo ClinicManagement of sickle cell anemia is usually aimed at avoiding pain episodes, relieving symptoms and preventing complications. Treatments might include medicines and blood transfusions. For some children and teenagers, a stem cell transplant might cure the disease.
- Sickle cell disease - WikipediaThe most common type is known as sickle cell anaemia. It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to a rigid, sickle-like shape under certain circumstances. Problems in sickle cell disease typically begin around 5 to 6 months of age.
- Sickle cell anemia - Symptoms & causes - Mayo ClinicIn sickle cell anemia, some red blood cells are shaped like sickles or crescent moons. These sickle cells also become rigid and sticky, which can slow or block blood flow. The current approach to treatment is to relieve pain and help prevent complications of the disease.
- Sickle Cell Anemia - StatPearls - NCBI BookshelfSickle cell anemia is an inherited disorder of the globin chains that causes hemolysis and chronic organ damage. Sickle cell anemia is the most common form of sickle cell disease (SCD), with a lifelong affliction of hemolytic anemia requiring blood transfusions, pain crises, and organ damage.
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