For Professionals

When to Suspect VEXAS Syndrome: A Practical Guide for Clinicians

Since its discovery in 2020, VEXAS syndrome has rapidly emerged as an important cause of late-onset systemic inflammation associated with clonal hematopoiesis. The syndrome is increasingly recognised in patients previously labelled as having refractory autoimmune disease, relapsing polychondritis, or unexplained inflammatory syndromes with cytopenias.