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The Thalassemia Program at the Dana-Farber/Boston Children’s Cancer and Blood Disorders Center treats all forms of thalassemia, including thalassemia minor or trait, thalassemia intermedia and thalassemia major (Cooley’s anemia), as well as rare forms of the disease such as hemoglobin E-beta thalassemia and hemoglobin H-alpha thalassemia. Because of our innovative approach, we are one of only six programs designated as centers of excellence in thalassemia by the National Cooley’s Anemia Foundation and one of only seven centers sponsored by the federal Centers for Disease Control and Prevention for the prevention of thalassemia complications.
Dana-Farber/Boston Children’s is an integrated pediatric hematology and oncology partnership between Dana-Farber Cancer Institute and Boston Children’s Hospital. We offer, in one specialized program, the full spectrum of services that are needed for diagnosis, treatment and ongoing care of even the rarest and hard-to-treat conditions.
The Thalassemia Program is staffed by a diverse team of thalassemia specialists, including experts in hematology, transfusion medicine and genetics. Because of the complexity of the disease, other medical specialists, including cardiologists, endocrinologists and gastroenterologists, are also part of the team. A full-time nurse practitioner coordinates care for our patients and their families.
Scientists and clinicians in our Thalassemia Program are developing new methods for the diagnosis and treatment of the disease, including new drugs and treatment options, as well as studying the genes that prevent hemoglobin production, a hallmark of thalassemia.
Learn more about our Thalassemia Program on the Dana-Farber/Boston Children’s website.
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