Sickle cell anemia is a genetic blood disorder characterized by the production of abnormal hemoglobin, known as hemoglobin S, which causes red blood cells to form a rigid, crescent or "sickle" shape. These misshapen cells can block blood flow in small vessels, leading to pain, organ damage, and increased risk of infections. The condition is inherited in an autosomal recessive pattern, meaning an individual must receive two copies of the sickle cell gene, one from each parent, to develop the disease. Treatment often focuses on managing symptoms and preventing complications, including pain management, blood transfusions, and hydroxyurea therapy.
It sounds like you are looking for Sickle Cell Anemia.
You get Sickle-Cell Anemia by Birth,it is a genetic disorder.
Yes, Sickle Cell Anemia is in fact a genetic disorder.
Mutations in the hemoglobin molecules cause sickle cell anemia.
Sickle cell anemia is genetic. It is an autosomal recessive disease.
An example of point-mutation is sickle-cell anemia. Sickle-cell disease is hereditary.
Sickle cell anemia is an autosomal recessive disease. Carriers have sickle cell trait, which confers resistance to malaria.
While technically there are more than one, the main one by far is sickle cell anemia.
An example of point-mutation is sickle-cell anemia. Sickle-cell disease is hereditary.
Sickle cell anemia is not sex linked.
i think is quantitative because we have less HB synthesized a or b globin ....qualitative, is the sikle cell anemias, where there is abnormality in Hb
sickle cell anemia