Syndrome in question

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-11-03T15:27:38Z
dc.date.available2015-11-03T15:27:38Z
dc.date.created2015-11-03T15:27:38Z
dc.date.issued2014-01-01
dc.identifierAnais Brasileiros de Dermatologia. Rio de Janeiro: Soc Brasileira Dermatologia, v. 89, n. 1, p. 177-179, 2014.
dc.identifier0365-0596
dc.identifierhttp://hdl.handle.net/11449/129898
dc.identifier10.1590/abd1806-4841.20142615
dc.identifierS0365-05962014000100177
dc.identifierWOS:000333043300030
dc.identifierS0365-05962014000100177.pdf
dc.identifier2543633050941005
dc.description.abstractThe authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises. MAGIC syndrome (mouth and genital ulcers with inflamed cartilage) is rare and groups together patients with this clinical picture without necessarily fulfilling the clinical criteria for Behçet's disease or relapsing polychondritis, demonstrating an independent disorder.
dc.languageeng
dc.publisherSociedade Brasileira de Dermatologia
dc.relationAnais Brasileiros de Dermatologia
dc.relation0.884
dc.relation0,520
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectBehcet syndrome
dc.subjectPolychondritis
dc.subjectRelapsing
dc.subjectStomatitis
dc.subjectAphthous
dc.subjectVasculitis
dc.titleSyndrome in question
dc.typeArtículos de revistas


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