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

Internet

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

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