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Jihane El Mandour, Cherraqi A, Jroundi L, Laamrani FZ
Osteopoekilosis is a rare hereditary sclerosing bone dysplasia, which was described simultaneously by Albers- SchÃnberg and Ledoux-Lebard in 1916, characterized by the Individualization of multiple small, homogeneous, well-defined bony lesions of rounded or oval form in the juxta-articular regions.