Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh
- PMID: 35950585
- DOI: 10.1080/03630269.2021.2008957
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh
Abstract
Bangladesh is a country with a population of 160 million with a gross national income per capita of US$1580.00. The major health problems in Bangladesh include acute respiratory infection, pneumonia, dengue fever, malaria and water-borne diseases. The health care system in Bangladesh is divided into primary secondary and tertiary levels, with each level having their own breakdown of available hospital beds and other treatment facilities. Thalassemia is a major health problem in Bangladesh. There are two types of thalassemia in Bangladesh: β-thalassemia (β-thal) and Hb E (HBB: c.79G>A)/β-thal, with the prevalence rate of β-thal trait being 4.1% and Hb E trait 6.1%. This study discusses spectrum types of thalassemia and hemoglobinopathies in Bangladesh and the types of carrier detection. The distribution of common mutations of thalassemia are also discussed and the distribution frequencies of genotypes and alleles of β-thal and Hb E patients are also compared. Additionally, we also conducted a study of the spectrum of thalassemia using high performance liquid chromatography (HPLC) of the tribal populations and analyzed the findings in our discussion. The results of these studies show that the phenotypic and genotypic presentation in Bangladesh is highly diverse. To properly understand this, we have to conduct an epidemiological survey of the population. Furthermore, there also has to be improvement on the awareness of thalassemia among the population to properly equip themselves to survive this disease.
Keywords: Bangladesh; hemoglobinopathy; overview; thalassemia.
Similar articles
-
Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Hemoglobin. 2016. PMID: 26635043 Review.
-
Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh.Hemoglobin. 2015;39(6):389-92. doi: 10.3109/03630269.2015.1078810. Epub 2015 Sep 24. Hemoglobin. 2015. PMID: 26402558
-
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program.Hemoglobin. 2022 Sep;46(5):285-289. doi: 10.1080/03630269.2022.2142608. Epub 2022 Nov 11. Hemoglobin. 2022. PMID: 36367309
-
Prevalence and Management of β-Thalassemia in India.Hemoglobin. 2022 Jan;46(1):27-32. doi: 10.1080/03630269.2021.2001346. Epub 2022 Feb 7. Hemoglobin. 2022. PMID: 35129043 Review.
-
Molecular Epidemiology of Hemoglobinopathies in Cambodia.Hemoglobin. 2016 Jun;40(3):163-7. doi: 10.3109/03630269.2016.1158723. Hemoglobin. 2016. PMID: 27117566
Cited by
-
Thalassemia: A Review of the Challenges to the Families and Caregivers.Cureus. 2022 Dec 13;14(12):e32491. doi: 10.7759/cureus.32491. eCollection 2022 Dec. Cureus. 2022. PMID: 36523854 Free PMC article. Review.
-
Health-related quality of life among thalassemia patients in Bangladesh using the SF-36 questionnaire.Sci Rep. 2023 May 12;13(1):7734. doi: 10.1038/s41598-023-34205-9. Sci Rep. 2023. PMID: 37173392 Free PMC article.
-
Prevalence of thalassemia-carrier couples and fertility risk assessment.Int J Hematol. 2024 Apr;119(4):374-382. doi: 10.1007/s12185-024-03722-2. Epub 2024 Feb 27. Int J Hematol. 2024. PMID: 38411864
-
Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with α-globin gene triplication.PeerJ. 2023 May 3;11:e15308. doi: 10.7717/peerj.15308. eCollection 2023. PeerJ. 2023. PMID: 37159832 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources