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Imaging of Gorlin-Goltz syndrome: Series of 2 cases
Gorlin–Goltz syndrome (GGS) is a rare autosomal dominant disorder with multisystemic involvement. It is characterized by the triad of multiple baso-cellular epitheliomas, odontogenic keratocysts (OKC) in the jaws and skeletal anomalies. Later, it was found that calcification of falx is also highly s...
Autores principales: | Rafiq, Suhail, Manzoor, Farzana, Dar, Musaib Ahmad, Aslam, Rassieq |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491327/ https://www.ncbi.nlm.nih.gov/pubmed/34703144 http://dx.doi.org/10.4103/0973-029X.325261 |
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