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

Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with <i>JAK2</i> V617F, <i>U2AF1</i> and <i>SETBP1</i> 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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Bibliographic Details
Main Authors: Sholhui Park, Min-Kyung So, Min-Sun Cho, Dae-Young Kim, Jungwon Huh
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Diagnostics
Subjects:
case report
primary myelofibrosis
paroxysmal nocturnal hemoglobinuria
<i>JAK2</i> V617F
<i>U2AF1</i> mutation
<i>SETBPT1</i> mutation
Online Access:https://www.mdpi.com/2075-4418/11/9/1644

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