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A Unique Case of Popliteal Artery Thrombosis in Isolated Prothrombin Gene Mutation
A prothrombin gene mutation (PTGM) is the second common cause of inherited thrombophilia after factor V Leiden. Hypercoagulable conditions have traditionally been reported to cause venous thrombosis, while arterial thrombosis is a rare occurrence. Studies have reported cases of preexisting hypercoag...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845479/ https://www.ncbi.nlm.nih.gov/pubmed/33527057 http://dx.doi.org/10.7759/cureus.12376 |