Statistical Indicators of Patients With Large and Intermittent β-thalassemia in Different Regions of Azerbaijan

Abstract

This article is devoted to the study of β-thalassemia, which is one of the most widespread hereditary diseases among the population of the Azerbaijan Republic. The possibilities of β-thalassemia manifestation together with abnormal forms of hemoglobin in the Azerbaijan population are traced. Basic prevention methods and the importance of establishing a State register of β-thalassemia cases are reviewed.