Beta-thalassemia natural history, complications and prognosis
|
Beta-thalassemia Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Beta-thalassemia natural history, complications and prognosis On the Web |
|
American Roentgen Ray Society Images of Beta-thalassemia natural history, complications and prognosis |
|
FDA on Beta-thalassemia natural history, complications and prognosis |
|
CDC on Beta-thalassemia natural history, complications and prognosis |
|
Beta-thalassemia natural history, complications and prognosis in the news |
|
Blogs on Beta-thalassemia natural history, complications and prognosis |
|
Risk calculators and risk factors for Beta-thalassemia natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Maryam Hadipour, M.D.[2]
Overview
Without regular blood transfusions, affected individuals by major beta-thalassemia typically develop severe anemia and related complications early in life, while beta-thalassemia intermedia patients would have a variable clinical course, complications, and prognosis. Beta-thalassemia minor subjects would not have significant symptoms, while in some cases might have an increased risk for iron deficiency anemia. Iron overload complications happen in transfusion-dependent thalassemia.