Abstract
The prevalence and molecular basis of β-thalassemia in the district of Isparta were determined in a total of 6,054 healthy high school students who were recruited from 21 randomly selected high schools in the Isparta province and region. In 182 subjects, naked eye single tube red cell osmotic fragility test (NESTROFT test) was positive HbA2 was measured by high-performance liquid chromatography (HPLC) in these subjects and was found to be high in 149 subjects. The incidence of β-thalassemia was 149 in 6,054 (25%). The β-thalassemia frequency was lower in the city center than in neighboring towns, 1.7% vs. 2.2%, respectively. The most prevalent mutation of β-thalassemia in this region was IVS 1-110 (G-A), followed by Codon 39 (C-T) and IVSII-745 (C-G).
Keywords: hemoglobinopathy, prevalence, β-thalassemia trait, screening, population
Copyright and license
Copyright © 2002 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY), which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.
How to cite
1.
Tunç B, Çetin H, Gümrük F, et al. The prevalence and molecular basis of β-thalassemia in Isparta province and region. Turk J Pediatr 2002; 44: 18-20. https://doi.org/10.24953/turkjpediatr.2002.2930