Cargando…

Gorlin Syndrome

Gorlin Syndrome, a rare genodermatosis, otherwise known as Nevoid basal cell carcinoma syndrome (NBCCS) is a multisystem disease affecting skin, nervous system, eyes, endocrine glands, and bones. It is characterized by multiple basal cell carcinomas, palmoplantar pits, jaw cysts, and bony deformitie...

Descripción completa

Detalles Bibliográficos
Autores principales: Devi, Basanti, Behera, Binodini, Patro, Sibasish, Pattnaik, Subhransu S, Puhan, Manas R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667306/
https://www.ncbi.nlm.nih.gov/pubmed/23723494
http://dx.doi.org/10.4103/0019-5154.110853
_version_ 1782271478644867072
author Devi, Basanti
Behera, Binodini
Patro, Sibasish
Pattnaik, Subhransu S
Puhan, Manas R
author_facet Devi, Basanti
Behera, Binodini
Patro, Sibasish
Pattnaik, Subhransu S
Puhan, Manas R
author_sort Devi, Basanti
collection PubMed
description Gorlin Syndrome, a rare genodermatosis, otherwise known as Nevoid basal cell carcinoma syndrome (NBCCS) is a multisystem disease affecting skin, nervous system, eyes, endocrine glands, and bones. It is characterized by multiple basal cell carcinomas, palmoplantar pits, jaw cysts, and bony deformities like kyphoscoliosis and frontal bossing. We would like to report a case of Gorlin syndrome with classical features, as this is a rare genodermatosis.
format Online
Article
Text
id pubmed-3667306
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-36673062013-05-30 Gorlin Syndrome Devi, Basanti Behera, Binodini Patro, Sibasish Pattnaik, Subhransu S Puhan, Manas R Indian J Dermatol E-Case Report Gorlin Syndrome, a rare genodermatosis, otherwise known as Nevoid basal cell carcinoma syndrome (NBCCS) is a multisystem disease affecting skin, nervous system, eyes, endocrine glands, and bones. It is characterized by multiple basal cell carcinomas, palmoplantar pits, jaw cysts, and bony deformities like kyphoscoliosis and frontal bossing. We would like to report a case of Gorlin syndrome with classical features, as this is a rare genodermatosis. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3667306/ /pubmed/23723494 http://dx.doi.org/10.4103/0019-5154.110853 Text en Copyright: © Indian Journal of Dermatology 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 E-Case Report
Devi, Basanti
Behera, Binodini
Patro, Sibasish
Pattnaik, Subhransu S
Puhan, Manas R
Gorlin Syndrome
title Gorlin Syndrome
title_full Gorlin Syndrome
title_fullStr Gorlin Syndrome
title_full_unstemmed Gorlin Syndrome
title_short Gorlin Syndrome
title_sort gorlin syndrome
topic E-Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667306/
https://www.ncbi.nlm.nih.gov/pubmed/23723494
http://dx.doi.org/10.4103/0019-5154.110853
work_keys_str_mv AT devibasanti gorlinsyndrome
AT beherabinodini gorlinsyndrome
AT patrosibasish gorlinsyndrome
AT pattnaiksubhransus gorlinsyndrome
AT puhanmanasr gorlinsyndrome