A Case of VEXAS: Vacuoles, E1 Enzyme, X-linked, Autoinflammatory, Somatic Syndrome With Co-existing DNA (Cytosine-5)-Methyltransferase 3A Mutation Complicated by Localized Skin Reaction to Tocilizumab and Azacitidine
Author:
Publisher
Springer Science and Business Media LLC
Subject
Aerospace Engineering
Reference19 articles.
1. Somatic mutations in UBA1 and severe adult-onset autoinflammatory disease;Beck DB;N Engl J Med,2020
2. Somatic mutations in rheumatological diseases: VEXAS syndrome and beyond;Sikora KA;Rheumatology (Oxford),2022
3. Somatic mutations in UBA1 define a distinct subset of relapsing polychondritis patients with VEXAS;Ferrada MA;Arthritis Rheumatol,2021
4. UBA1 and DNMT3A mutations in VEXAS syndrome. A case report and literature review;Shaukat F;Mod Rheumatol Case Rep,2022
5. Clonal hematopoiesis and VEXAS syndrome: survival of the fittest clones?;Kusne Y;Semin Hematol,2021
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1. Successful treatment with fludarabine and cyclophosphamide in a VEXAS syndrome patient with associated myelodysplastic syndrome: a case report and systematic review;Frontiers in Oncology;2024-04-11
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