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Vacuoles, E1 Enzyme, X-linked, Autoinflammatory, and Somatic (VEXAS) Syndrome: A Case Report
Maheen Zaidi1, Foster West1, Zachary Ellis1
1Internal Medicine, Baptist Memorial Hospital, Oxford, USA.
Cureus
|March 5, 2025
Summary
VEXAS syndrome, a condition linked to UBA1 mutations, presents uniquely in a 76-year-old male. Early UBA1 mutation testing is crucial for timely diagnosis and improved outcomes in this rare autoinflammatory disorder.
Area of Science:
- Hematology
- Immunology
- Genetics
Background:
- VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) is a recently identified autoinflammatory disorder.
- It primarily affects older men and is associated with somatic mutations in the UBA1 gene.
- VEXAS syndrome presents with hematologic and inflammatory symptoms, including cytopenias, fevers, and an increased risk of myelodysplastic syndrome (MDS).
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