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Article

DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndrome.

Arthritis and rheumatism - 1 Aug 2013

Ozçakar Z Birsin, Foster Joseph, Diaz-Horta Oscar, Kasapcopur Ozgur, Fan Yao-Shan, Yalçınkaya Fatoş, Tekin Mustafa

Abstract excerpt

OBJECTIVE: Hypocomplementemic urticarial vasculitis syndrome (HUVS) is characterized by recurrent urticaria along with dermal vasculitis, arthritis, and glomerulonephritis. Systemic lupus erythematosus (SLE) develops in >50% of patients with HUVS, although the pathogenesis is unknown. The aim of this study was to identify the causative DNA mutations in 2 families with autosomal-recessive HUVS, in order to reveal...

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PMID: 23666765
DOI: 10.1002/art.38010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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