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dc.contributor.authorKone-Paut, Isabelle
dc.contributor.authorShahram, Fahrad
dc.contributor.authorDarce-Bello, Martha
dc.contributor.authorCantarini, Luca
dc.contributor.authorCimaz, Rolando
dc.contributor.authorGattorno, Marco
dc.contributor.authorAnton, Jordi
dc.contributor.authorHofer, Michael
dc.contributor.authorChkirate, Bouchra
dc.contributor.authorBouayed, Kenza
dc.contributor.authorTugal-Tutkun, Ilknur
dc.contributor.authorKuemmerle-Deschner, Jasmin
dc.contributor.authorAgostini, Helene
dc.contributor.authorFederici, Sylvia
dc.contributor.authorArnoux, Armelle
dc.contributor.authorPiedvache, Celine
dc.contributor.authorOzen, Seza
dc.date.accessioned2019-12-10T10:35:26Z
dc.date.available2019-12-10T10:35:26Z
dc.date.issued2016
dc.identifier.issn0003-4967
dc.identifier.urihttps://doi.org/10.1136/annrheumdis-2015-208491
dc.identifier.urihttp://hdl.handle.net/11655/13878
dc.description.abstractBackground We aimed to describe the main features of Behcet's disease (BD) in children in the largest prospective cohort to date and to propose a classification. Methods An international expert consensus group was formed to define a data set of minimal symptoms for the inclusion of patients. Patients were entered prospectively during 66 months. Experts classified patients on a consensus basis. The concordance of two international classifications was analysed in confirmed patients with BD. Comparisons of subgroups of patients helped define consensus criteria. BD-associated clinical manifestations were also investigated in three control diseases extracted from an independent data set (Eurofever). Findings In total, 42 centres from 12 countries included 230 patients; data for 219 (M/F ratio=1) could be analysed. The experts classified 156 patients (71.2%) as having confirmed BD. Males more often than females showed cutaneous, ocular and vascular symptoms and females more often genital aphthosis. Age at disease onset and skin and vascular involvement were lower for European than non-European children. Oral aphthosis was the presenting sign for 81% (179/219) of patients. The mean delay to the second symptom was 2.9 +/- 2.2 years. International classifications were not concordant with the expert classification. Our paediatric classification contains six categories, a minimum of three signs (each in a distinct category) defining paediatric BD. Three clinical signs discriminated our cohort from the Eurofever cohorts. Interpretation We present a comprehensive description of a large cohort of patients from both European and non-European countries and propose the first classification of paediatric BD for future therapeutic trials.
dc.language.isoen
dc.publisherBMJ
dc.relation.isversionof10.1136/annrheumdis-2015-208491
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectRheumatology
dc.titleConsensus Classification Criteria For Paediatric Behcet'S Disease From A Prospective Observational Cohort: Pedbd
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalAnnals Of The Rheumatic Diseases
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume75
dc.identifier.issue6
dc.identifier.startpage958
dc.identifier.endpage964
dc.description.indexWoS


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