Document Type : Case Report(s)
Authors
1 Department of Rheumatology, Shiraz University of Medical Sciences, Shiraz
2 Department of Ophthalmology, Shiraz University of Medical Sciences, Shiraz
Abstract
Osteogenesis Imperfecta (OI) is a genetic disorder characterized by bones that break easily, often from little or no apparent cause. In this article, we present a patient suffering from OI, who had concomitant active Behçet’s Disease(BD)with repeated oro-genital ulcers, skin postular eruptions and severe recurrent bilateral uveitis. This patient, is, to our knowledge the first reported case in literature.
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