Hematology and Blood Disorders

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Hematology and Blood Disorders 44 7897 074717

Severe Thalassemia Disease Scholarly Peer Review Journal

Thalassemia is an inherited blood disease during which the body makes an abnormal sort of hemoglobin. Hemoglobin is that the molecule in red blood cells that carries oxygen. The disorder leads to excessive destruction of red blood cells, which results in anemia. Anemia may be a condition during which your body doesn’t have enough normal, healthy red blood cells. Thalassemia is inherited,  that means at least one of your parents must be a carrier of the disorder. It’s caused by either a mutation or a deletion of certain key gene fragments. Thalassemia minor may be a less serious sort of the disorder. There are two main sorts of thalassemia that are more serious. In alpha thalassemia, a minimum of one among the alpha globin genes features a mutation or abnormality.

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