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First two cases of craniomaxillofacial fibrous dysplasia from Nepal – case series
Fibrous dysplasia is a benign fibro-osseous disease of the bone, which is most commonly associated with congenital mutations in cAMP regulating protein Gsα coded by GNAS-1 gene. Often it is seen involving the craniofacial skeleton and can range from an asymptomatic monostotic form to polyostotic var...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263244/ https://www.ncbi.nlm.nih.gov/pubmed/30538581 http://dx.doi.org/10.2147/CCIDE.S178599 |