Article
VEXAS syndrome: lessons learnt from an early Australian case series.
Internal medicine journal - 1 Apr 2022
Islam Sadia, Cullen Taylor, Sumpton Daniel, Damodaran Arvin, Heath David, Bosco Annmarie, Doo Nicole W, Kidson-Gerber Giselle, Cheong Anthony, Lawford Ron, Walsh Rebecca, Sammel Anthony
Abstract excerpt
VEXAS is a newly recognised adult-onset autoinflammatory syndrome resulting from a somatic mutation in the UBA1 gene. Herein, we present three cases of VEXAS syndrome in Sydney, Australia, that capture key clinical features and the refractory nature of the condition. They highlight the importance of multidisciplinary collaboration for early diagnosis and the need for new therapeutic options.
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