Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5681482 | Medicine - Programa de Formación Médica Continuada Acreditado | 2016 | 11 Pages |
Abstract
Hemolytic anemias are grouped in two big categories: hereditary HA, due to a half-life reduction of red cells as consequence to congenital structural defects (membranopathies, erythro-enzymopathies, thalassemia and hemoglobinopathies); and acquired HA which are divided in immune and non-immune mediated, highlighting its frequency the autoimmune anemias and its severity the thrombotic microangiopathies. Its distinctive features require different management strategies.
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Authors
M. Berenguer Piqueras, V. Cabañas Perianes, M. Moya Arnao, E. Salido Fiérrez,