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Association of Behçet’s Disease with Osteogenesis Imperfecta in A Ten-Year-Old Girl | ||
| Iranian Journal of Medical Sciences | ||
| مقاله 17، دوره 26، 3-4، اسفند 2001، صفحه 171-173 اصل مقاله (480.54 K) | ||
| نوع مقاله: Case Report(s) | ||
| نویسندگان | ||
| Sh. Samangooei* 1؛ S.M. Hakim1؛ M. Mehryar2 | ||
| 1Department of Rheumatology, Shiraz University of Medical Sciences, Shiraz | ||
| 2Department of Ophthalmology, Shiraz University of Medical Sciences, Shiraz | ||
| چکیده | ||
| 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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