Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study
Wójcik Sylwia, Koszowski Rafał, Drozdowska Bogna and 2 more
Open Medicine · 2016
doi:10.1515/med-2016-0082 (opens in a new tab)
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Abstract
McCune Albright syndrome (MCA) is a rare complication of genetic origin. The authors present a case study of a patient with MCA diagnosed with multifocal fibrous dysplasia in his limb and craniofacial bones. The symptoms of the disease in the patient’s facial and oral tissue and the treatment administered have been described.
Abstract licence: CC BY-NC-ND
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