Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report

Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. It is characterized by multiple disorders involving multiple systems. We present a case of 11-year-old male child presenting with multiple odontogenic keratocyst to the dental clinic. Retrograde diagnosis of Gorlin...

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Autores principales: Acharya, Sonu, Panda, Swagatika, Singh Dhull, Kanika, Sahoo, Sujit Ranjan, Ray, Prayas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086603/
https://www.ncbi.nlm.nih.gov/pubmed/25206225
http://dx.doi.org/10.5005/jp-journals-10005-1221
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author Acharya, Sonu
Panda, Swagatika
Singh Dhull, Kanika
Sahoo, Sujit Ranjan
Ray, Prayas
author_facet Acharya, Sonu
Panda, Swagatika
Singh Dhull, Kanika
Sahoo, Sujit Ranjan
Ray, Prayas
author_sort Acharya, Sonu
collection PubMed
description Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. It is characterized by multiple disorders involving multiple systems. We present a case of 11-year-old male child presenting with multiple odontogenic keratocyst to the dental clinic. Retrograde diagnosis of Gorlin-Goltz syndrome was made after clinical and radiological investigation. How to cite this article: Acharya S, Panda S, Dhull KS, Sahoo SR, Ray P. Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report. Int J Clin Pediatr Dent 2013;6(3):208-212.
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spelling pubmed-40866032014-09-09 Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report Acharya, Sonu Panda, Swagatika Singh Dhull, Kanika Sahoo, Sujit Ranjan Ray, Prayas Int J Clin Pediatr Dent Case Report Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. It is characterized by multiple disorders involving multiple systems. We present a case of 11-year-old male child presenting with multiple odontogenic keratocyst to the dental clinic. Retrograde diagnosis of Gorlin-Goltz syndrome was made after clinical and radiological investigation. How to cite this article: Acharya S, Panda S, Dhull KS, Sahoo SR, Ray P. Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report. Int J Clin Pediatr Dent 2013;6(3):208-212. Jaypee Brothers Medical Publishers 2013 2013-10-14 /pmc/articles/PMC4086603/ /pubmed/25206225 http://dx.doi.org/10.5005/jp-journals-10005-1221 Text en Copyright © 2013; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Acharya, Sonu
Panda, Swagatika
Singh Dhull, Kanika
Sahoo, Sujit Ranjan
Ray, Prayas
Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title_full Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title_fullStr Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title_full_unstemmed Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title_short Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
title_sort gorlin syndrome with bilateral polydactyly: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086603/
https://www.ncbi.nlm.nih.gov/pubmed/25206225
http://dx.doi.org/10.5005/jp-journals-10005-1221
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