Association of Behçet’s Disease with Osteogenesis Imperfecta in A Ten-Year-Old Girl

Sh. Samangooei, S.M. Hakim, M. Mehryar

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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pISSN: 0253-0716         eISSN: 1735-3688