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VEXAS syndrome: lessons learnt from an early Australian case series
Sadia Islam1, Taylor Cullen2, Daniel Sumpton1
1Rheumatology Department, Concord Repatriation General Hospital, Sydney, New South Wales, Australia.
Abstract:
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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