Cherubism: best clinical practice

Cherubism is a skeletal dysplasia characterized by bilateral and symmetric fibro-osseous lesions limited to the mandible and maxilla. In most patients, cherubism is due to dominant mutations in the SH3BP2 gene on chromosome 4p16.3. Affected children appear normal at birth. Swelling of the jaws usual...

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Detalles Bibliográficos
Autores principales: Papadaki, Maria E, Lietman, Steven A, Levine, Michael A, Olsen, Bjorn R, Kaban, Leonard B, Reichenberger, Ernst J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359956/
https://www.ncbi.nlm.nih.gov/pubmed/22640403
http://dx.doi.org/10.1186/1750-1172-7-S1-S6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359956/
https://www.ncbi.nlm.nih.gov/pubmed/22640403
http://dx.doi.org/10.1186/1750-1172-7-S1-S6

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