{"paper_id":"21fb8711-dcc1-44bf-9adf-cf703c6f8265","body_text":"European Journal of Dermatology\nMENUEndometriosis in the setting of Muckle-Wells syndrome treated with an IL-1β antagonist Volume 27, numéro 4, July-August 2017\nIllustrations\nDepartment of Dermatology,\nUniversity of Occupational and Environmental Health,\n1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555,\nJapan\nUniversity of Occupational and Environmental Health,\n1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555,\nJapan\n- DOI : 10.1684/ejd.2017.3052\n- Page(s) : 442-3\n- Année de parution : 2017\nCryopyrin-associated autoinflammatory syndrome (CIAS) is characterized by a triad of rash, arthropathy, and central nervous system involvement [1]. Chronic infantile neurological cutaneous articular syndrome (CINCA), Muckle-Wells syndrome, and familial cold autoinflammatory syndrome have been shown to be allelic, caused by heterozygous mutations in the CIAS gene, NLPR3, on chromosome 1q44, which encodes a pyrin-like protein [2]. Interleukin (IL)-1 antagonists are emerging as an effective therapy [...]","source_license":"CC0","license_restricted":false}