VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis
Open Access
- 1 September 2025
- journal article
- Published by KEAI Publishing in Genes & Diseases
- Vol. 12 (5) , 101540
Abstract
No abstract availableFunding Information
- Health Commission of Hunan Province
- National Natural Science Foundation of China
- Hunan Provincial Natural Science Foundation
This publication has 4 references indexed in Scilit:
- Serious infections in patients with VEXAS syndrome: data from the French VEXAS registryAnnals of the Rheumatic Diseases, 2023
- VEXAS syndrome complicated with severe infectionRheumatology, 2022
- VEXAS syndrome in myelodysplastic syndrome with autoimmune disorderExperimental Hematology & Oncology, 2021
- Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory DiseaseNew England Journal of Medicine, 2020