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The most common type is known as sickle cell anemia. 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.
Jun 11, 2019 · Symptoms. Types. Risk factors. Complications. Diagnosis. Treatment. Outlook. What is sickle cell anemia? Sickle cell anemia, or sickle cell disease (SCD), is a genetic disease of the red...
Dec 22, 2022 · Management 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.
Apr 22, 2024 · Last 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 disease (SCD) is an inherited blood disorder that causes “sickle” shaped red blood cells that can stick together, blocking blood flow and oxygen from reaching all parts of the body.
People have anemia and sometimes jaundice. Pain in the long bones, abdomen, and chest can indicate sickle cell crisis. Worsening anemia, fever, shortness of breath, and low oxygen levels can indicate acute chest syndrome, a major complication of sickle cell disease.
Oct 3, 2023 · Sickle cell disease (SCD) is a group of inherited red blood cell disorders. In SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle.” People with SCD can live full lives and enjoy most of the activities that other people do. If you have SCD, it’s important to learn how to stay as healthy as possible.
