Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study

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. 
DOI: 10.1515/med-2016-0082

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