Ear, Nose, Throat, and Bronchial Involvements in VEXAS Syndrome

Author:

Beaumesnil Stacy1,Boucher Sophie23,Lavigne Christian1,Urbanski Geoffrey13,Lacombe Valentin13

Affiliation:

1. Department of Internal Medicine and Clinical Immunology, Angers University Hospital, Angers, France

2. Department of Otorhinolaryngology (ENT), Angers University Hospital, Angers, France

3. Mitolab Team, CNRS 6214 - INSERM 1083, MITOVASC Institute, University of Angers, Angers, France

Publisher

American Medical Association (AMA)

Subject

Otorhinolaryngology,Surgery

Reference6 articles.

1. Somatic mutations in UBA1 and severe adult-onset autoinflammatory disease.;Beck;N Engl J Med,2020

2. Further characterization of clinical and laboratory features occurring in VEXAS syndrome in a large-scale analysis of multicenter case-series of 116 French patients.;Georgin-Lavialle;Br J Dermatol,2021

3. Somatic mutations in UBA1 define a distinct subset of relapsing polychondritis patients with VEXAS.;Ferrada;Arthritis Rheumatol,2021

4. Severe joint involvement in VEXAS syndrome: a case report.;Lacombe;Ann Intern Med,2021

5. Vacuoles in neutrophil precursors in VEXAS syndrome: diagnostic performances and threshold.;Lacombe;Br J Haematol,2021

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