What are the diagnostic features of VEXAS syndrome?
VEXAS syndrome is diagnosed primarily through genetic testing for UBA1 mutations and supported by characteristic laboratory and clinical findings, including bone marrow vacuolization and systemic inflammatory symptoms. Evidence is limited, and diagnosis can be complex due to mimicry of other conditions.
Authors
- Tripdatabase
Publication Details
- Journal
- Zenodo (CERN European Organization for Nuclear Research)
- Published
- 2026-11-06
- DOI
- https://doi.org/10.5281/zenodo.24012650
- Primary Topic
- Immunodeficiency and Autoimmune Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00