Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5641833 | Journal of Oral and Maxillofacial Surgery | 2016 | 6 Pages |
Abstract
Gnathodiaphyseal dysplasia (GDD) is a rare hereditary syndrome characterized by cemento-ossifying fibromas of the maxillary bones, fragile bones, curvature and cortical thinning of the tubular bones, and diaphyseal sclerosis of the long bones. In this study, 2 complex clinical cases of 2 members of the same family had GDD and were treated in the authors' odonto-stomatology department. The first was treated with a block bone graft and implant-prosthetic therapy; the other, who had extensive osteomyelitis of the second quadrant, was managed with extraction of the involved teeth, surgical revision of the site, and a graft of autologous platelet concentrate.
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Authors
Alberto MD, DMD, Joseph DMD, MDS, Luca DMD, Paolo MD, DMD,