Clinical, pathological, and genetic evaluations of Chinese patient with otodental syndrome and multiple complex odontoma: Case report

Otodental syndrome is a rare autosomal-dominant disease characterized by globodontia, associated with sensorineural, high-frequency hearing loss. Here, we describe the clinical, pathological, and genetic evaluations of a 9-year-old girl with otodental syndrome and multiple complex odontoma. The pati...

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Detalles Bibliográficos
Autores principales: Liu, Anqi, Wu, Meiling, Guo, Xiaohe, Guo, Hao, Zhou, Zhifei, Wei, Kewen, Xuan, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
5900
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293465/
https://www.ncbi.nlm.nih.gov/pubmed/28151902
http://dx.doi.org/10.1097/MD.0000000000006014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293465/
https://www.ncbi.nlm.nih.gov/pubmed/28151902
http://dx.doi.org/10.1097/MD.0000000000006014

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