Beta-Thalassemia Learning Center2017-04-06T20:22:09+00:00

How is Beta-Thalassemia treated?

Treatment for beta-thalassemia varies depending on the severity of the disorder. People with beta-thalassemia major and intermedia should be monitored through regular hematological evaluations. During pregnancy, illness or infection, there is a higher chance of [...]

How is Beta-Thalassemia diagnosed?

Beta-thalassemia is diagnosed using genetic testing and blood tests. Genetic testing DNA testing of the HBB gene can be used to diagnose beta-thalassemia. The beta-thalassemia DNA test detects the most common HBB genetic mutations known [...]

What are the signs and symptoms of Beta-Thalassemia?

The signs and symptoms of beta-thalassemia can vary in severity depending on the extent of HBB gene deficiencies. The severity of the disease is classified into three types in the order of decreasing severity: β-thalassemia [...]

What causes Beta-Thalassemia?

Beta-thalassemia is caused by genetic mutations in the HBB gene which affect the production of β-globin. Insufficient β-globin decreases the amount of functional hemoglobin (HbA), thereby decreasing the amount of red blood cells for maturation. [...]

What is Beta-Thalassemia?

Beta-thalassemia is an inherited blood disorder characterized by low levels of hemoglobin, leading to anemia and insufficient oxygen supply to the body. Common symptoms include jaundice, fatigue, organ damage, and delayed growth and development. Hemoglobin [...]