Beta thalassemia is a treatable blood disorder that’s inherited, or passed down through your genes. With beta thalassemia, your body doesn’t make enough hemoglobin, which is an important ...

An essential factor in distinguishing thalassemia phenotypes is transfusion dependence. While beta-thalassemia major requires ...

There are various types of thalassemia, depending on the genetic features present. Alpha and beta tend to be more common, but there are others. Alpha-globin and beta-globin protein chains make up ...

Problems with hemoglobin production occur in people with thalassemia because these genes affect how the body makes two proteins: Alpha globin and beta globin. These proteins are the two major ...

Beta-thalassemia, also known as β-thalassemia is a genetic disorder marked by reduced or absent beta chain synthesis of hemoglobin, leading to ineffective erythropoiesis and severe anemia.

You most likely have beta thalassemia minor (one normal gene and one that causes low beta-cell-chain production), which consists of mild anemia and very small cells. This condition can look very ...

You most likely have beta thalassemia minor (one normal gene and one that causes low beta-cell-chain production), which consists of mild anemia and very small cells. This condition can look very ...

Exagamglogene autotemcel (exa-cel) (Casgevy®) is a gene therapy for treating sickle cell disease in patients 12 years and older with recurrent vaso-occlusive crises and transfustion-dependent beta ...