Hb S disease; Hemoglobin S Disease; Herrick's anemia; SCD
Sickle cell anemia is an inherited disease in which the red blood cells, normally disc-shaped, become crescent shaped. As a result, they function abnormally and cause small blood clots. These clots give rise to recurrent painful episodes called "sickle cell pain crises."
A tissue with red blood cells, white blood cells, platelets, and other substances suspended in fluid called plasma. Blood takes oxygen and nutrients to the tissues, and carries away wastes.
Sickle Cell Anemia as related to Blood
- Sickle Cell Anemia - KidsHealth - the Web's most …
Signs and Symptoms. Teens with sickle cell anemia may develop jaundice (pronounced: jon-dis), a condition that results from the high rate of red blood cell …
- Sickle Cell Anemia: MedlinePlus - National Library of ...
Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. The cells are shaped like a crescent or sickle.
- Sickle-cell disease - Wikipedia, the free encyclopedia
Sickle-cell disease (SCD), also known as sickle-cell anaemia (SCA) and drepanocytosis, is a hereditary blood disorder, characterized by an abnormality in the …
- What Is Sickle Cell Anemia? - NHLBI, NIH
Sickle cell anemia (sickle cell disease) is a disorder of the blood caused by an inherited abnormal hemoglobin (the oxygen-carrying protein within the red blood cells).
- Sickle cell anemia: MedlinePlus Medical Encyclopedia
Sickle cell anemia is a disease passed down through families. The red blood cells that are normally shaped like a disc take on a sickle or crescent shape.
- Sickle Cell Disease (Sickle Cell Anemia) Symptoms, …
Pain crises in persons with sickle cell anemia are intermittent painful episodes that are the result of inadequate blood supply to body tissues.
- Do You Know About Sickle Cell Anemia? - KidsHealth - …
Signs and Symptoms. Kids who have sickle cell anemia may feel pain in their chest, stomach, or bones when blood vessels get clogged with sickle cells.
- Sickle Cell Anemia News -- ScienceDaily
Read articles summarizing medical research on sickle-cell anemia.
- Blood Journal | Fetal hemoglobin in sickle cell anemia
Abstract. Fetal hemoglobin (HbF) is the major genetic modulator of the hematologic and clinical features of sickle cell disease, an effect mediated by its exclusion ...