Systemic thrombosis with prothrombin Belgrade mutation in a Chinese patient: A case report
This case strengthens our understanding about hereditary basis of thrombophilia and provokes considerations for therapeutic options on prothrombin Belgrade mutation.
Authors
- Baohui Weng (ORCID: https://orcid.org/0000-0002-9625-2522)
- Yan Huang (ORCID: https://orcid.org/0000-0001-7607-9585)
- Shan Deng
- Zhen Li (ORCID: https://orcid.org/0000-0002-9783-169X)
- Liya Pan (ORCID: https://orcid.org/0009-0004-2980-8633)
- Yanfeng Wu (ORCID: https://orcid.org/0000-0002-0601-4206)
Institutions
- Tianjin Medical University General Hospital (CN)
- Liuzhou Maternal and Child Health Hospital (CN)
- Liuzhou General Hospital (CN)
- Guangxi Zhuang Autonomous Region Brain Hospital (CN)
Publication Details
- Journal
- World Journal of Clinical Cases
- Published
- 2024-12-18
- DOI
- https://doi.org/10.12998/wjcc.v13.i10.98390
- Citations
- 1
- Primary Topic
- Blood Coagulation and Thrombosis Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.45