Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature

Primary myelofibrosis (PMF) and paroxysmal nocturnal hemoglobinuria (PNH) are very rare diseases, respectively, and it is uncommon to have both diseases together. Mutational profiling using next-generation sequencing in PMF and PNH detected additional mutations associated with myeloid neoplasms, sug...

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Detalles Bibliográficos
Autores principales: Park, Sholhui, So, Min-Kyung, Cho, Min-Sun, Kim, Dae-Young, Huh, Jungwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466901/
https://www.ncbi.nlm.nih.gov/pubmed/34573985
http://dx.doi.org/10.3390/diagnostics11091644

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466901/
https://www.ncbi.nlm.nih.gov/pubmed/34573985
http://dx.doi.org/10.3390/diagnostics11091644

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