Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients*

Georgin‐Lavialle, Sophie; Terrier, Benjamin; F. Guédon, Alexis; Heiblig, Maël; Comont, T.; Lazaro, Estibaliz; Lacombe, Valentin; Terriou, Louis; Ardois, Samuel; Bouaziz, Jean‐David; Mathian, Alexis; Le Guenno, G.; Aouba, Achille; Outh, R.; Meyer, A.; Roux‐Sauvat, Marielle; Ebbo, Mikaël; Zhao, Lin‐Pierre; Bigot, Adrien; Jamilloux, Yvan; Guillotin, Vivien; Flamarion, Edouard; Henneton, Pierrick; Vial, Guillaume; Jachiet, Vincent; Rossignol, Julien; Vinzio, S.; Weitten, Thierry; Vinit, J.; Deligny, C.; Humbert, S.; Samson, Maxime; Magy‐Bertrand, N.; Moulinet, T.; Bourguiba, R.; Hanslik, Thomas; Bachmeyer, Claude; Sébert, Marie; Kostine, Marie; Bienvenu, Boris; Biscay, P.; Liozon, É.; Sailler, L.; Chasset, François; Audemard‐Verger, Alexandra; Duroyon, Eugénie; Sarrabay, Guillaume; Borlot, Felippe; Diéval, C.; Cluzeau, Thomas; Marianetti, Paola; Lobbes, Hervé; Boursier, Guilaine; Gerfaud‐Valentin, Mathieu; Jeannel, Juliette; Servettaz, Amélie; Audia, Sylvain; Larue, M.; Henriot, Basile; Faucher, B.; Graveleau, J.; De Sainte Marie, B.; Galland, Joris; Bouillet, Laurence; Arnaud, Catherine; Adès, Lionel; Carrat, Fabrice; Hirsch, Pierre; Fenaux, Pierre; Fain, O.; Sujobert, Pierre; Kosmider, Olivier; Mékinian, A.; VEXAS group, French; GFM, CEREMAIA, MINHEMON, GFEV,

doi:10.1111/bjd.20805

Public

Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients*

Published in British Journal of Dermatology • Oct 11, 2021

Authors:

Sophie Georgin‐Lavialle

Benjamin Terrier

Alexis F. Guédon

Abstract

BACKGROUND: A new autoinflammatory syndrome related to somatic mutations of UBA1 was recently described and called VEXAS syndrome ('Vacuoles, E1 Enzyme, X-linked, Autoinflammatory, Somatic syndrome'). OBJECTIVES: To describe clinical characteristics, laboratory findings and outcomes of VEXAS syndrom...

Subject

Medicine

Internal medicine

Monoclonal gammopathy of undetermined significance

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