Work

What are the diagnostic features of VEXAS syndrome?

Year: 2026

Type: article

Abstract: 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.

Source: Zenodo (CERN European Organization for Nuclear Research)

DOI: 10.5281/zenodo.24012650

Author: Tripdatabase

Language: English

Topic: Immunodeficiency and Autoimmune Disorders

Subfield: Immunology

Field: Immunology and Microbiology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W7225390707

FWCI:

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Related to: 10