A patient with Camurati-Engelmann disease presenting bilateral TMJ ankylosis: A case report

Camurati-Engelmann Disease (CED), also known as progressive diaphyseal dysplasia, is a rare congenital disorder inherited in an autosomal-dominant pattern, most commonly affecting the skull and diaphysis of long tubular bones. Clinical symptoms start in early age and include ostealgia, muscle atroph...

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Detalles Bibliográficos
Autores principales: Salman, Nour J., Pimenta e Souza, Denis, Kuriki, Erika, Sant’Ana, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452382/
https://www.ncbi.nlm.nih.gov/pubmed/32841778
http://dx.doi.org/10.1016/j.ijscr.2020.08.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452382/
https://www.ncbi.nlm.nih.gov/pubmed/32841778
http://dx.doi.org/10.1016/j.ijscr.2020.08.006

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