Alpha Thalassemia

Alpha Thalassemia

What is alpha thalassemia?

Thalassemia is an inherited disorder that affects the production of normal hemoglobin (a type of protein in red blood cells that carries oxygen to the tissues of the body). Thalassemia includes a number of different forms of anemia, including the alpha thallasemias. The severity and type of anemia depends upon the number of genes that are affected.

What causes alpha thalassemia?

Alpha thalassemia is caused by mutations in the alpha chain of the hemoglobin molecule. Normally, there are two genes coding for the alpha chain on each #16 chromosome, for a total of four genes. The alpha chain is an important component of fetal hemoglobin (usually made before birth) and hemoglobin A and hemoglobin A2 (present after birth). How these genes are altered determines the specific type of alpha thalassemia in a person:

How is alpha thalassemia diagnosed?

Alpha thalassemia is most commonly found in Africa, the Middle East, India, Southeast Asia, southern China, and the Mediterranean region. Carrier status can be suggested by the following:

All of these studies can be performed from a single blood sample. Prenatal diagnosis is determined from CVS (chorionic villus sampling) or amniocentesis. Confirmation of alpha thalassemia requires DNA analysis.

Treatment for alpha thalassemia

Specific treatment for alpha thalassemia will be determined by your doctor based on:

Treatment may include:

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