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Eklem Hastalik Cerrahisi. 2013;24(1):46-8. doi: 10.5606/ehc.2013.11.

A new syndrome mimicking Jaffe-Campanacci syndrome: a case report.

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Department of Orthopedics and Traumatology, Medical Faculty of Eskişehir Osmangazi University, 26480 Meşelik, Eskişehir, Turkey.


Jaffe-Campanacci syndrome (JCS) is a well-known condition with its clinical and radiological characteristics. Extraskeletal congenital anomalies of this syndrome include café-au-lait spots, mental retardation, cardiovascular abnormalities, ocular deformities, hypogonadism or cryptorchidism. Multiple non-ossifying fibromas are also characteristic bone lesions. In this article, we present a new syndrome mimicking JCS, which is characterized by a simple bone cyst and extraskeletal lesions.

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