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Kindler's syndrome: A rare case report
Kindler syndrome is a rare hereditary disorder, associated with skin fragility. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes a 16-year-old patient with classical features...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067787/ https://www.ncbi.nlm.nih.gov/pubmed/24963250 http://dx.doi.org/10.4103/0976-237X.132342 |
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author | Suman, Neelam Kaur, Simrat Kaur, Supreet Sarangal, Vandana |
author_facet | Suman, Neelam Kaur, Simrat Kaur, Supreet Sarangal, Vandana |
author_sort | Suman, Neelam |
collection | PubMed |
description | Kindler syndrome is a rare hereditary disorder, associated with skin fragility. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes a 16-year-old patient with classical features like blistering and photosensitivity in childhood and the subsequent development of poikiloderma. |
format | Online Article Text |
id | pubmed-4067787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40677872014-06-24 Kindler's syndrome: A rare case report Suman, Neelam Kaur, Simrat Kaur, Supreet Sarangal, Vandana Contemp Clin Dent Case Report Kindler syndrome is a rare hereditary disorder, associated with skin fragility. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes a 16-year-old patient with classical features like blistering and photosensitivity in childhood and the subsequent development of poikiloderma. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4067787/ /pubmed/24963250 http://dx.doi.org/10.4103/0976-237X.132342 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 Suman, Neelam Kaur, Simrat Kaur, Supreet Sarangal, Vandana Kindler's syndrome: A rare case report |
title | Kindler's syndrome: A rare case report |
title_full | Kindler's syndrome: A rare case report |
title_fullStr | Kindler's syndrome: A rare case report |
title_full_unstemmed | Kindler's syndrome: A rare case report |
title_short | Kindler's syndrome: A rare case report |
title_sort | kindler's syndrome: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067787/ https://www.ncbi.nlm.nih.gov/pubmed/24963250 http://dx.doi.org/10.4103/0976-237X.132342 |
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