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A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited
De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities. We present here an account of 5-year follow-up since the birth of an Indian boy wit...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763701/ https://www.ncbi.nlm.nih.gov/pubmed/26955101 http://dx.doi.org/10.4103/0019-5154.174031 |
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author | Dutta, Abhijit Ghosh, Sudip Kumar Ghosh, Arghyaprasun Roy, Sutirtha |
author_facet | Dutta, Abhijit Ghosh, Sudip Kumar Ghosh, Arghyaprasun Roy, Sutirtha |
author_sort | Dutta, Abhijit |
collection | PubMed |
description | De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities. We present here an account of 5-year follow-up since the birth of an Indian boy with DBS, who had a few rare and unusual manifestations. In addition, our case probably represents the first reported case of DBS from India. |
format | Online Article Text |
id | pubmed-4763701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47637012016-03-07 A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited Dutta, Abhijit Ghosh, Sudip Kumar Ghosh, Arghyaprasun Roy, Sutirtha Indian J Dermatol Case Report De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities. We present here an account of 5-year follow-up since the birth of an Indian boy with DBS, who had a few rare and unusual manifestations. In addition, our case probably represents the first reported case of DBS from India. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4763701/ /pubmed/26955101 http://dx.doi.org/10.4103/0019-5154.174031 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Dutta, Abhijit Ghosh, Sudip Kumar Ghosh, Arghyaprasun Roy, Sutirtha A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title | A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title_full | A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title_fullStr | A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title_full_unstemmed | A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title_short | A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited |
title_sort | 5-year journey with cutis laxa in an indian child: the de barsy syndrome revisited |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763701/ https://www.ncbi.nlm.nih.gov/pubmed/26955101 http://dx.doi.org/10.4103/0019-5154.174031 |
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