Our Alpha thalassemia Main Article provides a comprehensive look at the who, what, when and how of Alpha thalassemia

Definition of Alpha thalassemia

Alpha thalassemia: A blood disorder, thalassemia is not one disease but rather a group of disorders that have a single feature in common: they all have a genetic defect in the production of hemoglobin, the protein that enables red blood cells to carry oxygen.

All forms of hemoglobin are made up of two molecules: heme and globin. Globin is made up of 4 polypeptide chains. In normal adult hemoglobin (Hb A), the predominant type of hemoglobin after the first year of life, 2 of the globin polypeptide chains are identical to one another and are designated the alpha chains. The other 2 chains are also identical to one another but differ from the alpha chains and are termed the beta chains. In fetal hemoglobin (Hb F), the predominant hemoglobin during fetal development, there are 2 alpha chains and 2 different chains called gamma chains.

The problem in the thalassemias is with globin production. The thalassemias are classified according to the type of globin polypeptide chain that is underproduced. The alpha chain is involved in alpha thalassemia (and the beta chain is affected in the more familiar beta thalassemia).

In alpha thalassemia, the heterozygous state (with a single gene for alpha thalassemia) is innocuous or harmless. There are no symptoms or at most mild anemia, because there is another gene still able to make alpha chains.

However, the homozygous state (with both genes for alpha thalassemia) is lethal before birth because no alpha chains can be made and without alpha chains, there can be no Hb F or Hb A and without Hb F or Hb A, the inevitable result is an unsuccessful pregnancy.

Common Misspellings: alpa thalassemia

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