A novel HBD gene mutation associated with normal-range hb A2 in β-thalassemia carriers
β-thalassemia is one of the most common single-gene inherited conditions in the world, prevalence of β-thalassaemia in south China is 3–4%,increased Hb A2 level is one of the most important markers of β-thalassemia heterozygous carriers.Interaction of HBD gene defect with β-thalassemia can result in the normal Hb A2 β-thalassemia, potentially leading to a misdiagnosis of β- thalassemia carrier state. This study aimed to identify a novel mutation in HBD gene resulted in normal Hb A2 levels in β-thalassemia carriers, and explore the underlying mechanism of the novel HBD gene mutation using a minigene splicing assay and in vivo validation.
Authors
- wenlan Liu
- Ming Chang
- Chao Liu
- Lijun Zhang
- Lei Zhang
- Shan Duan
- Jingxin Yang
- Xingping Li
- Yang Liu
Institutions
- Sun Yat-sen University (CN)
- The Seventh Affiliated Hospital of Sun Yat-sen University (CN)
- Shenzhen Maternity and Child Healthcare Hospital (CN)
- Shenzhen University Health Science Center (CN)
Publication Details
- Journal
- Annals of Hematology
- Published
- 2026-03-02
- DOI
- https://doi.org/10.1007/s00277-026-06892-7
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Sanming Project of Medicine in Shenzhen