Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review

Inherited thrombophilia is an important cause of venous thrombosis. The Factor V Leiden (FVL) is the most commonly encountered mutation, followed by the prothrombin G20210A gene mutation (PTM). The typical venous thrombotic events (VTEs) associated with PTM mutations are deep vein thrombosis (DVT) a...

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Detalles Bibliográficos
Autores principales: Elkattawy, Sherif, Alyacoub, Ramez, Singh, Kerry S., Fichadiya, Hardik, Kessler, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016586/
https://www.ncbi.nlm.nih.gov/pubmed/35426321
http://dx.doi.org/10.1177/23247096211058486

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016586/
https://www.ncbi.nlm.nih.gov/pubmed/35426321
http://dx.doi.org/10.1177/23247096211058486

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