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Thalassaemia

Definition: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Synonyms (terms occurring on more labels are shown first): thalassemia, thalassaemia

More information: PubMed search and possibly Wikipedia

Drugs with this indication