disease can be a very scary issue to deal with however, with proper monitoring and care, many people are able to live their life to its full capacity with minor complications.“Sickle cell disease is a group of inherited red blood cell disorders that affect hemoglobin, the protein that carries oxygen through the body. Normally, red blood cells are disc-shaped and flexible enough to move easily through the blood vessels.
In the United States, most people who have sickle cell disease are of African ancestry or identify themselves as Black:, KPRC 2 spoke with Medical Director, Dr. Idowu, at UT Physicians Comprehensive Sickle Cell Center and asked the following questions.A: Sickle cell disease is an inherited group of blood disorders that causes red blood cells to become misshapen or sickle-shaped.
SEE ALSO: Katy teen becomes first sickle cell disease patient in Texas Medical Center to become her own donor A: Acute pain crisis, severe anemia, stroke, bone infarct, splenic infarct, risks for infections, retinal damage, priapism, leg ulcers, heart problems, lung problems , kidney disease, liver complication and multiple organ dysfunction or even multiple organ failure.A: Bone marrow transplant, also known as stem cell transplant, offers the only potential cure for sickle cell anemia. It’s typically reserved for people younger than age 16 because the risks increase for people older than 16.
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