SO Arab - Sickle Cell Disease
Also known as: Sickle cell hemoglobin 0 Arab disease, SO Arab disease.
What is SO Arab - sickle cell disease?
S O Arab - sickle cell disease is a variant of sickle cell disease, it is usually a mild form of sickle cell anemia that is prevalent among Arab populations. This causes the body’s hemoglobin, or red blood cells, to take on a sickle shape and not flow through the blood vessels as smoothly, which prevent red blood cells from carrying oxygen effectively. This can cause a number of complications.
What causes SO Arab - sickle cell disease?
S O Arab - sickle cell disease is a genetic disorder that is passed along from parents to their children. It’s a recessive genetic disorder, which means that both parents must pass along different genes in order for the child to develop the disorder.
What are the symptoms of SO Arab - sickle cell disease?
S O Arab - sickle cell disease often causes mild anemia
, tiredness or weakness. Occasionally, pain and stiffness in the arms, legs or back can occur as blood clumps up in the vessels. Others problems can include an increased risk of infection, an enlarged spleen, eye problems and more.
What are SO Arab - sickle cell disease care options?
Treatments typically involve preventing potential complications and treating them as they arise. People with the disorder receive continuous care to prevent and manage the complications of the disease.
Hydroxyurea is the main treatment for reducing complications. Education is essential to provide supportive and preventive care. The only cure for Sickle Cell disease is bone marrow transplantation; gene therapy will be a curative therapy and will be coming available soon.
Reviewed by: Athena Pefkarou, MD
This page was last updated on: September 30, 2020 04:40 PM
Dr. Athena Pefkarou discusses the approaches to treating sickle cell disease in this edition of Children's Health Chats.
Patient Success Stories
Oscar, 20, was born with Sickle Cell Disease, a condition that affects red blood cells (sickle cell anemia) and blockage of blood flow causing pain. The pain is often so severe; patients suffer painful bouts known as sickle cell crisis and often require hospitalization.
Learn more about
Sickle Cell Disease
Sickle cell disease is a group of familial red blood cell disorders. Sickle cell disease causes the red blood cells to be oddly shaped, and have difficulty flowing through the blood vessels properly which causes them to break up easily resulting in anemia and damage to the organs.
Blood and Marrow Transplantation
The transplantation of blood or bone marrow is the procedure of transferring and replacing the hematopietic stem cells.
Hydroxyurea is a medicine that can help children and adults with sickle cell disease.