Ocular Involvement in Muckle-Wells Syndrome. (2nd January 2020)

• Record Type: Journal Article
• Authors: Cekic, Sukru; Yalcinbayir, Ozgur; Kilic, Sara Sebnem
• Is Part Of: Ocular immunology and inflammation. Volume 28:Number 1(2020)
• Page Start: 70
• Page End: 78
• Publication Date: 2020-01-02
• Subjects: Autoinflammation -- conjunctivitis -- cryoprin -- Muckle Wells syndrome -- uveitis; Eye -- Diseases -- Immunological aspects -- Periodicals; Eye -- Inflammation -- Periodicals; 617.7
• DOI: 10.1080/09273948.2018.1552305
• Languages: English
• ISSNs: 0927-3948

Abstract

ABSTRACT: Purpose : To present the ocular findings of the members of a family that has the diagnosis of Muckle Wells syndrome, a form of cryopyrin associated periodic syndrome (CAPS). Materials and Methods : Nine patients with MWS were included in this study. Each study participant underwent a systemic evaluation, comprehensive ophthalmic examination, and auxillary testings. Results : In this study, conjunctivitis was the most prominent ocular finding. Other relatively common ocular findings included band keratopathy, clinical signs of past uveitis, and corneal topography abnormalities. Nystagmus, corneal leukoma, and optic nerve pallor with epiretinal membrane were also detected. Rare ocular manifestations were posterior stromal corneal opacification with edema, anterior iris snychecia, and mild cataract. Conclusion : MWS is a rare systemic autoinflammatory disorder that presents with a variety of ocular findings. Exacerbation of systemic and ocular findings with cold is a hallmark of the disease.