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Thalassemia

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Thalassemia major Thalassemia minor

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Thalassemia

Definition:

Thalassemias are hereditary disorders characterized by defective production of hemoglobin. This leads to low production, and excessive destruction, of red blood cells.

Alternative Names:
Thalassemia; Mediterranean anemia; Cooley's anemia

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Causes, incidence, and risk factors:

Hemoglobin contains two chains, alpha and beta globin. Genetic defects may be inherited that cause an imbalance in the production of either chain.

Beta thalassemias are caused by a mutation in the beta globin chain. Genes must be inherited from both parents to acquire the major form of this disease. If one gene is inherited, the person will be a carrier of the disease, but will not have symptoms. This is the minor form of the disease.

In the major form, children are normal at birth, but develop anemia during the first year of life. Growth failure, bone deformities, and enlarged liver and spleen are some of the problems that can occur. Blood transfusions may modify some of the disease manifestation, but iron overload from the transfusions may cause damage to the heart, liver, and endocrine systems.

The mild form of beta thalassemia produces small red blood cells, with no symptoms. Risk factors include a family history of thalassemia and an ethnic background that has shown susceptibility to the disease.

Beta thalassemias occur in people of Mediterranean origin, and to a lesser extent, Chinese, other Asians, and blacks.

Alpha thalassemias occur most commonly in people from southeast Asia and China, and are caused by deletion of a gene or genes from the alpha globin chain. The most severe form of alpha thalassemia causes stillbirth (death of a fetus before delivery).

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