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VEXAS syndrome: Clinical manifestations, diagnosis, and treatment.

Reumatologia clinica - 1 Jan 2024

Loeza-Uribe Michelle Patricia, Hinojosa-Azaola Andrea, Sánchez-Hernández Beatriz E, Crispín José C, Apodaca-Chávez Elia, Ferrada Marcela A, Martín-Nares Eduardo

Abstract excerpt

VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is an adult-onset autoinflammatory syndrome characterized by somatic mutations in the UBA1 gene and is considered the prototype of hematoinflammatory diseases. Patients with VEXAS syndrome exhibit inflammatory and hematological manifestations that can lead to clinical diagnoses such as relapsing polychondritis, polyarteritis nodosa, Sweet...

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Identifiers

PMID: 38160120
DOI: 10.1016/j.reumae.2023.12.004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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