A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic Review
This study provides valuable insights for genetic counseling, prenatal diagnosis, and potential therapeutic strategies for aHUS patients with <i>CFB</i> mutations.
Authors
- Huijun Yuan (ORCID: https://orcid.org/0000-0002-4173-7688)
- Fengxiao Bu (ORCID: https://orcid.org/0000-0002-4882-4856)
- Xicui Long (ORCID: https://orcid.org/0000-0001-9728-7842)
- Yu Lu (ORCID: https://orcid.org/0000-0003-3944-1252)
- Hao-Ran Lei
- Peng Wan (ORCID: https://orcid.org/0000-0002-3560-4969)
Institutions
- Sichuan University (CN)
- West China Hospital of Sichuan University (CN)
- Chengdu University of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- Case Reports in Nephrology and Dialysis
- Published
- 2025-08-14
- DOI
- https://doi.org/10.1159/000547975
- Primary Topic
- Complement system in diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Sichuan University
- West China Hospital, Sichuan University