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Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome

Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria. Dentist plays a major role in the diagnosis of this dis...

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Autores principales: Manjima, S., Naik, Zameera, Keluskar, Vaishali, Bagewadi, Anjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374303/
https://www.ncbi.nlm.nih.gov/pubmed/25821359
http://dx.doi.org/10.4103/0976-237X.152959
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author Manjima, S.
Naik, Zameera
Keluskar, Vaishali
Bagewadi, Anjana
author_facet Manjima, S.
Naik, Zameera
Keluskar, Vaishali
Bagewadi, Anjana
author_sort Manjima, S.
collection PubMed
description Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria. Dentist plays a major role in the diagnosis of this disease due to the oral and maxillofacial manifestations of the syndrome. In some cases, jaw cysts are diagnosed by routine radiographs advised by the dentists. Odontogenic keratocysts in such syndromic patients will be multiple and extensive and in some cases results in cortical expansion and facial disfigurement. Thorough clinical examination and investigations prompt an early confirmation of the syndrome, which is very essential to avoid morbidity associated with the syndrome. Here, we report a case of multiple odontogenic cysts in a 16-year-old patient which later was diagnosed as a case of Gorlin Goltz syndrome.
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spelling pubmed-43743032015-03-27 Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome Manjima, S. Naik, Zameera Keluskar, Vaishali Bagewadi, Anjana Contemp Clin Dent Case Report Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria. Dentist plays a major role in the diagnosis of this disease due to the oral and maxillofacial manifestations of the syndrome. In some cases, jaw cysts are diagnosed by routine radiographs advised by the dentists. Odontogenic keratocysts in such syndromic patients will be multiple and extensive and in some cases results in cortical expansion and facial disfigurement. Thorough clinical examination and investigations prompt an early confirmation of the syndrome, which is very essential to avoid morbidity associated with the syndrome. Here, we report a case of multiple odontogenic cysts in a 16-year-old patient which later was diagnosed as a case of Gorlin Goltz syndrome. Medknow Publications & Media Pvt Ltd 2015-03 /pmc/articles/PMC4374303/ /pubmed/25821359 http://dx.doi.org/10.4103/0976-237X.152959 Text en Copyright: © Contemporary Clinical Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Manjima, S.
Naik, Zameera
Keluskar, Vaishali
Bagewadi, Anjana
Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title_full Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title_fullStr Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title_full_unstemmed Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title_short Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
title_sort multiple jaw cysts-unveiling the gorlin-goltz syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374303/
https://www.ncbi.nlm.nih.gov/pubmed/25821359
http://dx.doi.org/10.4103/0976-237X.152959
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