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

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 admini...

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Detalles Bibliográficos
Autores principales: Wójcik, Sylwia, Koszowski, Rafał, Drozdowska, Bogna, Śmieszek-Wilczewska, Joanna, Raczkowska-Siostrzonek, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329869/
https://www.ncbi.nlm.nih.gov/pubmed/28352837
http://dx.doi.org/10.1515/med-2016-0082
Descripción
Sumario: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.

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