Familial Essential Thrombocythemia With Novel MPL L502G and G208K Mutations

Familial essential thrombocythemia is characterized by the inheritance of germline mutations to progeny, thereby increasing the risk for the development of essential thrombocythemia. Here, we present two cases of young women who developed thromboembolic phenomena, one of whom with an ischemic event ...

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Detalles Bibliográficos
Autores principales: Rendo, Matthew, Cavacece, Christian, Kou, Chung-ting J, Beeler, Bradley W, Fenderson, Joshua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012324/
https://www.ncbi.nlm.nih.gov/pubmed/35449633
http://dx.doi.org/10.7759/cureus.23220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012324/
https://www.ncbi.nlm.nih.gov/pubmed/35449633
http://dx.doi.org/10.7759/cureus.23220

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