VEXAS-genvarianter forklarer tidligere uerkendt klinisk syndrom

Translated title of the contribution: VEXAS gene variants explain previously unrecognized clinical syndrome

Mads Nyhuus Bendix Rasch, Fruzsina Szabados, Jens Magnus Bernth Jensen, Kirstine Overgaard Nielsen, Ellen-Margrethe Hauge, Anne Troldborg*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

17 Downloads (Pure)

Abstract

This review aims to make clinicians aware of the newly described syndrome, VEXAS. VEXAS should become an obvious differential diagnosis in cases of unexplained inflammation, anemia, and rheumatological and/or hematological manifestations. Patients with VEXAS are typically male aged > 60, with inflammation, and macrocytic anaemia. On suspicion of cancer or infections patients have frequently been exposed to extensive diagnostic procedures and hospital admissions. In this review, we summarise the current knowledge of VEXAS regarding pathogenesis, symptoms, diagnosis, and treatment.

Translated title of the contributionVEXAS gene variants explain previously unrecognized clinical syndrome
Original languageDanish
Article numberV03220225
JournalUgeskrift for Læger
Volume184
ISSN0041-5782
Publication statusPublished - 3 Oct 2022

Fingerprint

Dive into the research topics of 'VEXAS gene variants explain previously unrecognized clinical syndrome'. Together they form a unique fingerprint.

Cite this