Cherubism: a rare case report with literature review

Cherubism is an autosomal dominant disorder caused by a mutation of the gene encoding the binding protein SH3BP2. However, non-hereditary forms are observed, probably related to a de novo mutation. It is clinically manifested by an enlargement or a deformation of the jaw associated with a malpositio...

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Detalles Bibliográficos
Autores principales: Lahfidi, A., Traore, W.M., Diallo, I.D., Lrhorfi, N., Elhaddad, S., Allali, N., Chat, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388877/
https://www.ncbi.nlm.nih.gov/pubmed/35991385
http://dx.doi.org/10.1016/j.radcr.2022.07.063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388877/
https://www.ncbi.nlm.nih.gov/pubmed/35991385
http://dx.doi.org/10.1016/j.radcr.2022.07.063

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