Diagnostic Challenges and Importance of Genetic Testing in α/β Thalassaemia: A Case Report
1. IntroductionThe thalassaemias are a group of inherited haematological disorders caused by defects in the synthesis of one or more of the globin chains. It is an autosomal recessive disorder and affects men and women equally. Approximately 5% of the
Authors
- Mohammed Mejbahuddin Mia (ORCID: https://orcid.org/0000-0001-7098-5974)
- Ahmedyar Hasan (ORCID: https://orcid.org/0000-0001-6182-3551)
- Sheikh Anisul Haque (ORCID: https://orcid.org/0000-0002-0927-4126)
- S. R. Hoque (ORCID: https://orcid.org/0009-0008-1942-239X)
- Md Imrul Kaes
Institutions
- Dinajpur Medical College (BD)
Publication Details
- Published
- 2025-09-03
- DOI
- https://doi.org/10.22541/au.174906370.08873232/v2
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00