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Behçet’s disease (BD) is a multi-systemic disease with heterogeneous clinical features1. Its manifestations appear one after another during the course of the disease with attacks and remissions2-4. Some involvements such as mucous lesions seem to appear early, and others such as gastrointestinal (GI), vascular, and central nervous system (CNS) involvements many years later5, 6. The aim of this study was to investigate the chronology of different manifestations of BD during its course.