Beta Thalassemia & Sickle Cell Screening
Confirm Beta Thalassemia State with complete information on Mutations
Beta Thalassemia is a common inherited blood Disorder that reduces production of hemoglobin due to mutation in one or bothcopies of beta globin gene (HBB). HBB gene produces globin protein which is a part of Hemoglobin. The severity of anemia caused by Beta Thalassemia depends on which mutations are present.