Mayo Clinic Marketplace Check out these best-sellers and special offers on books and newsletters from Mayo Clinic. Red blood cells usually live for about 120 days before they need to be replaced.
Clinical Trials. The pain varies in intensity and can last for a few hours to a few weeks. More research is needed to find out why some people with SCT have complications and others do not. Inheritance of hemoglobin genes from parents with sickle cell trait and hemglobin C trait.
What is sickle cell disease? Sickle cell disease SCD is a group of inherited red blood cell disorders.
This can cause pain and other serious problems such infection, acute chest syndrome and stroke. If you get one, you might need to go to the hospital for treatment.
It increases the amount of fetal hemoglobin in the blood. Bone marrow or stem cell transplants are very risky, and can have serious side effects, including death.
When this happens, oxygen can't reach nearby tissues. Living With. Get Screened for Sickle Cell Trait.
This medicine is not safe during pregnancy.
Centers for Disease Control and Prevention. Some people have only a few pain episodes. Safety and effectiveness of antimalarial therapy in sickle cell disease:... This content does not have an Arabic version.
Section Navigation. What are the treatments for sickle cell disease? For the transplant to work, the bone marrow must be a close match. Share on: It most often is found at birth during routine newborn screening tests at the hospital.