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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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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 |
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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 |