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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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
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author Rafiq, Suhail
Manzoor, Farzana
Dar, Musaib Ahmad
Aslam, Rassieq
author_facet Rafiq, Suhail
Manzoor, Farzana
Dar, Musaib Ahmad
Aslam, Rassieq
author_sort Rafiq, Suhail
collection PubMed
description 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 specific. We present radiological findings in case series of two cases, one with multiple OKC, calcified falx, skin lesions, and fibrous dysplasia of sphenoid and second with multiple OKC, calcified falx, vertebral anomaly and medulloblastoma.
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spelling pubmed-84913272021-10-25 Imaging of Gorlin-Goltz syndrome: Series of 2 cases Rafiq, Suhail Manzoor, Farzana Dar, Musaib Ahmad Aslam, Rassieq J Oral Maxillofac Pathol Case Report 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 specific. We present radiological findings in case series of two cases, one with multiple OKC, calcified falx, skin lesions, and fibrous dysplasia of sphenoid and second with multiple OKC, calcified falx, vertebral anomaly and medulloblastoma. Medknow Publications & Media Pvt Ltd 2021 2021-08-31 /pmc/articles/PMC8491327/ /pubmed/34703144 http://dx.doi.org/10.4103/0973-029X.325261 Text en Copyright: © 2021 Journal of Oral and Maxillofacial Pathology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Rafiq, Suhail
Manzoor, Farzana
Dar, Musaib Ahmad
Aslam, Rassieq
Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title_full Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title_fullStr Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title_full_unstemmed Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title_short Imaging of Gorlin-Goltz syndrome: Series of 2 cases
title_sort imaging of gorlin-goltz syndrome: series of 2 cases
topic Case Report
url 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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