 The study concluded that alpha-falicemia was highly prevalent in the study area, with 4.43% of the population affected by the condition. Additionally, 95% of the cases had deletion or non-deletion mutations in the alpha-globin gene, while only 5% were negative for any of the 21 mutations tested. This article was authored by Mohammed Saibor, Abdullah Ahmed Mubarki, Hassan Abdul Hamali, and others.