Three years of follow-up of otodental syndrome in 3-year-old Chinese boy: a rare case report

BACKGROUND: Otodental syndrome is an exceptionally rare autosomal dominant condition characterized by a delayed eruption of posterior teeth, globodontia, lisping, and sensorineural hearing loss. In this case report, we reported a 3-year-old Chinese boy with the otodental syndrome. CASE PRESENTATION:...

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Detalles Bibliográficos
Autores principales: Su, Ji-mei, Zeng, Su-juan, Ye, Xiao-wei, Wu, Zhi-fang, Huang, Xin-wen, Pathak, Janak L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659250/
https://www.ncbi.nlm.nih.gov/pubmed/31345197
http://dx.doi.org/10.1186/s12903-019-0860-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659250/
https://www.ncbi.nlm.nih.gov/pubmed/31345197
http://dx.doi.org/10.1186/s12903-019-0860-z

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