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

Hemoglobin is the iron-rich protein ... and some people with this type may require occasional treatments (e.g., blood transfusions). Beta Thalassemia Major (Cooley's Anemia) Also known as ...

For beta thalassemia, the part of the hemoglobin molecule that's affected determines how serious your condition will be. Four genes are responsible for making the alpha protein. You get two from ...

Beta thalassemia minor—also known as beta thalassemia trait or B thalassemia—is a blood disorder. It lowers your blood’s level of hemoglobin, an iron-containing protein in red blood cells ...

You can also co-inherit thalassemia mutations with other hemoglobin gene problems, such as sickle cell trait. Interestingly, people with beta-thalassemia major who also inherit an α globin gene ...

There are two main types of thalassemia: alpha-thalassemia and beta-thalassemia. Most healthy hemoglobin includes two proteins: alpha-globin and two beta-globin. Inheriting faulty alpha-globin ...

For patients with beta thalassemia, the increase in fetal hemoglobin addresses the insufficient quantity ... research sent straight to your inbox with our monthly clinical updates e-newsletter ...

Sickle cell beta-thalassemia refers to an inherited condition that impacts hemoglobin. People with the condition have different changes in each copy of their hemoglobin gene. One causes red blood ...

With beta thalassemia, your body doesn’t make enough hemoglobin, which is an important protein used by red blood cells. If you don’t have enough hemoglobin, your red blood cells don’t work ...

Beta-thalassemia is a genetic disorder that occurs because of a mutation in the HBB gene. When a person has two copies of this mutation, their body produces less hemoglobin. Hemoglobin is a ...