Cargando…

Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report

Gorlin–Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routin...

Descripción completa

Detalles Bibliográficos
Autores principales: Chandran, Satheesh, Marudhamuthu, Karthikeyan, Riaz, R, Balasubramaniam, Saravanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dentmedpub Research and Printing Co 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516062/
https://www.ncbi.nlm.nih.gov/pubmed/26225111
_version_ 1782383008340246528
author Chandran, Satheesh
Marudhamuthu, Karthikeyan
Riaz, R
Balasubramaniam, Saravanan
author_facet Chandran, Satheesh
Marudhamuthu, Karthikeyan
Riaz, R
Balasubramaniam, Saravanan
author_sort Chandran, Satheesh
collection PubMed
description Gorlin–Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routine radiographs. A patient presented with signs and symptoms of Gorlin–Goltz syndrome to us in her early stages.
format Online
Article
Text
id pubmed-4516062
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dentmedpub Research and Printing Co
record_format MEDLINE/PubMed
spelling pubmed-45160622015-07-29 Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report Chandran, Satheesh Marudhamuthu, Karthikeyan Riaz, R Balasubramaniam, Saravanan J Int Oral Health Case Report Gorlin–Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routine radiographs. A patient presented with signs and symptoms of Gorlin–Goltz syndrome to us in her early stages. Dentmedpub Research and Printing Co 2015 /pmc/articles/PMC4516062/ /pubmed/26225111 Text en Copyright: © Journal of International Oral Health 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
Chandran, Satheesh
Marudhamuthu, Karthikeyan
Riaz, R
Balasubramaniam, Saravanan
Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title_full Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title_fullStr Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title_full_unstemmed Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title_short Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report
title_sort odontogenic keratocysts in gorlin–goltz syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516062/
https://www.ncbi.nlm.nih.gov/pubmed/26225111
work_keys_str_mv AT chandransatheesh odontogenickeratocystsingorlingoltzsyndromeacasereport
AT marudhamuthukarthikeyan odontogenickeratocystsingorlingoltzsyndromeacasereport
AT riazr odontogenickeratocystsingorlingoltzsyndromeacasereport
AT balasubramaniamsaravanan odontogenickeratocystsingorlingoltzsyndromeacasereport