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Elucidating the spectrum of alpha-thalassemia mutations in Iran
Valeh Hadavi1, Amir Hossein Taromchi, Mahdi Malekpour
1Kariminejad-Najmabadi Pathology & Genetics Center, 14665/154, Tehran, Iran.
Abstract:
Alpha thalassemia (alpha-thal) is one of the most common hemoglobin (Hb) disorders in the world. Alpha-globin genes are located on chromosome 16. The majority of alpha-thal mutations are deletions but point mutations are found as well. Since the Iranian population is a mixture of different ethnic groups, frequency and distribution of alpha-globin mutations in various regions of the country need to be clarified. These findings can contribute to a wider understanding of this disorder.
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