Sickle Cell Anemia

Sickle Cell Anemia

What is sickle cell anemia? Sickle cell anemia is a hereditary chronic hemolytic anemia caused by the production of Hb S as a result of a mutation in codon 6 of the beta globin gene. This mutation causes the hemoglobin to sickle when the red cell is...
Beta Thalassemia

Beta Thalassemia

What is beta thalassemia?  Beta thalassemia is a genetic blood disorder that reduces the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Thalassemia is defined as the quantitative reduction of globin chains production...