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...

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Detalles Bibliográficos
Autores principales: Rafiq, Suhail, Manzoor, Farzana, Dar, Musaib Ahmad, Aslam, Rassieq
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2021
Materias:
Case Report
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

Internet

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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