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VEXAS Mimicking Antiphospholipid Syndrome: Diagnostic Challenges of False-Positive Antiphospholipid Antibodies
Sayeed Khan1, Hadia Eiman2, Sanober Nusrat3
1Department of Molecular and Cellular Physiology, Albany Medical College, Albany, NY 12208, USA.
Abstract:
Somatic UBA1-mutated VEXAS syndrome is now recognized as a multisystem disorder marked by diffuse systemic inflammation, refractory cytopenia with or without bone marrow dysplasia, and thrombotic events affecting both venous and arterial systems [...].
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