α-Thalassemia Mutations in Khuzestan Province, Southwest Iran

Abstract

Although α-thalassemia (α-thal) is the most common hereditary hemoglobin (Hb) disorder in Iran, no comprehensive data are so far available on the prevalence of the disease in the province of Khuzestan in Southwest Iran. This study investigates the spectrum of α-thal mutations in this region.

One hundred and twenty-one subjects from Khuzestan Province, Iran, were initially tested for the three most common Iranian α-thal mutations ( − α^3.7, − α^4.2, and − − ^MED) by gap-polymerase chain reaction (gap-PCR). Reverse hybridization test strips and DNA sequencing were used to identify additional α-globin mutations. A total of 131 mutated α-globin alleles were identified in these patients. Of the 13 mutations that were detected in Khuzestan Province, Iran, the − α^3.7 single gene deletion was the most frequently identified variant, representing 62.6% of the total; we also observed significant numbers of individuals with compound heterozygous mutations. On the basis of our results, we strongly recommend screening for the most common mutations to improve the molecular diagnosis of anemia in this region.

Keywords:

• α-Thalassemia (α-thal)
• Mutation
• Khuzestan Province
• Iran