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Sickle cell disease is a group of inherited blood disorders that affect the shape and function of red blood cells. It can cause pain, anemia, infections, stroke, and organ damage. Learn about the genetics, diagnosis, and management of sickle cell disease.
Vaso-occlusive crisis (VOC) is a complication of sickle cell anemia, a genetic disorder that affects red blood cells. VOC causes pain, organ damage, and sometimes death. Learn about the symptoms, diagnosis, and treatment of VOC.
In patients with sickle cell disease, red blood cells, which are usually disk-shaped, take on a crescent or sickle shape. This change can cause cells to clump together, leading to clots and ...
Sickle cell nephropathy is a type of kidney disease associated with sickle cell disease which causes kidney complications as a result of sickling of red blood cells in the small blood vessels. The hypertonic and relatively hypoxic environment of the renal medulla , coupled with the slow blood flow in the vasa recta , favors sickling of red ...
NEW HAVEN, Conn. (WTNH) — Sickle cell disease is an inherited blood disorder impacting 100,000 people in the U.S., disproportionately people of color. Dr. Lila Van Doren, assistant professor of ...
Acute chest syndrome is a complication of sickle cell anemia that causes lung inflammation and hypoxemia. It is not clear if it has a specific ICD-10 code, but it is often associated with fever, cough, pain, and low oxygen levels.
Sickle cell is an inherited and debilitating blood disorder that causes normal round red blood cells – which carry oxygen through the body – to become crescent-shaped and rigid.
Sickle cell trait is a condition where a person has one abnormal allele of the hemoglobin beta gene (genotype AS) and produces both normal and abnormal hemoglobin. It is associated with some resistance to malaria, but also rare complications such as sickle cell crisis, renal medullary carcinoma, and urinary tract infection.