Case Report: PROS1 (c.76+2_76+3del) pathogenic mutation causes pulmonary embolism
Hereditary thrombophilia caused by mutations in the PROS1 (c.76+2_76+3del) gene is extremely rare. In clinical practice, heparin and rivaroxaban treatment are beneficial.
Authors
- Meijie Yang (ORCID: https://orcid.org/0000-0001-5890-7324)
- Song Zhang (ORCID: https://orcid.org/0000-0002-9364-4053)
- Yuan Zhou (ORCID: https://orcid.org/0000-0002-5600-5754)
- Peng Ding (ORCID: https://orcid.org/0000-0003-0424-0186)
- Sheng Li (ORCID: https://orcid.org/0000-0003-0539-4961)
- Lijia Zhi (ORCID: https://orcid.org/0000-0002-2194-7442)
Institutions
- Chengdu University of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- Frontiers in Cardiovascular Medicine
- Published
- 2024-10-11
- DOI
- https://doi.org/10.3389/fcvm.2024.1459579
- Primary Topic
- Venous Thromboembolism Diagnosis and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00