Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children
After excluding potential influencing factors such as splenectomy, the anemia symptoms in ANK1-HS patients were more severe than those in SPTB-HS patients. However, there was no statistically significant difference in indicators between HS patients with different types of gene mutations.
Authors
- Xia Guo (ORCID: https://orcid.org/0000-0002-9283-3274)
- Ju Gao (ORCID: https://orcid.org/0000-0001-5893-9406)
- Huang Duowen
Institutions
- Sichuan University (CN)
- West China Second University Hospital of Sichuan University (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2025-08-20
- DOI
- https://doi.org/10.3389/fped.2025.1650295
- Primary Topic
- Erythrocyte Function and Pathophysiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00