Therapeutic options in VEXAS syndrome: insights from a retrospective series
Estelle Bourbon, Maël Heiblig, Mathieu Gerfaud Valentin, Thomas Barba, Cécile‐Audrey Durel, Jean‐Christophe Lega, Fiorenza Barraco, P. Sève, Yvan Jamilloux, Pierre Sujobert
Abstract
Bourbon et al describe a series of 19 patients from France with VEXAS syndrome, including a novel genetic aberration in UBA1, and the outcomes of treatment for those with and those without myelodysplasia.
Topics & Concepts
Series (stratigraphy)MedicineRetrospective cohort studyIntensive care medicineInternal medicineBiologyPaleontologyOtitis Media and Relapsing PolychondritisCoagulation, Bradykinin, Polyphosphates, and AngioedemaAutoimmune Bullous Skin Diseases