THALASSEMIA, BETA

Course overview

Beta-thalassemia refers to a group of autosomal recessive inherited disorders of Hgb synthesis (i.e., hemoglobinopathies) characterized by decreased synthesis of the beta-globin subunits of the Hgb molecule (as opposed to alpha-thalassemia, in which synthesis of the alpha-globin subunits are decreased). This continuing education module is designed to give the reader/learner an increased understanding of beta-thalassemia, including its clinical presentation, symptoms, and treatment, and to aid in caring for the patient with this diagnosis. Readers may explore any or all of the topics. One contact hour of continuing education credit is available for those who successfully complete the post-test and evaluation form.