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Limbal dermoid in Nager acrofacial dysostosis: A rare case report
Nager syndrome, also called preaxial acrofacial dysostosis, comprises two groups of defects involving the limbs and craniofacial region, respectively. This syndrome is rare and only 70 cases have been reported in the literature. The exact cause of this syndrome is unknown, but there is indication th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061675/ https://www.ncbi.nlm.nih.gov/pubmed/23619496 http://dx.doi.org/10.4103/0301-4738.111194 |
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author | Malik, Rohit Goel, Sumit Aggarwal, Saurabh |
author_facet | Malik, Rohit Goel, Sumit Aggarwal, Saurabh |
author_sort | Malik, Rohit |
collection | PubMed |
description | Nager syndrome, also called preaxial acrofacial dysostosis, comprises two groups of defects involving the limbs and craniofacial region, respectively. This syndrome is rare and only 70 cases have been reported in the literature. The exact cause of this syndrome is unknown, but there is indication that it is genetically based. Ocular manifestations of this syndrome include widely separated downward slanting eyes, absence of eyelashes, ptosis of upper eyelids and colobomas on the inner aspect of lower eyelids. We report limbal dermoid in a patient with Nager syndrome. We did not find such an association of “Limbal dermoid in Nager acrofacial dysostosis syndrome” on PubMed using Nager acrofacial dysostosis, limbal dermoid and ocular manifestations as the keywords. |
format | Online Article Text |
id | pubmed-4061675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40616752014-06-19 Limbal dermoid in Nager acrofacial dysostosis: A rare case report Malik, Rohit Goel, Sumit Aggarwal, Saurabh Indian J Ophthalmol Brief Communications Nager syndrome, also called preaxial acrofacial dysostosis, comprises two groups of defects involving the limbs and craniofacial region, respectively. This syndrome is rare and only 70 cases have been reported in the literature. The exact cause of this syndrome is unknown, but there is indication that it is genetically based. Ocular manifestations of this syndrome include widely separated downward slanting eyes, absence of eyelashes, ptosis of upper eyelids and colobomas on the inner aspect of lower eyelids. We report limbal dermoid in a patient with Nager syndrome. We did not find such an association of “Limbal dermoid in Nager acrofacial dysostosis syndrome” on PubMed using Nager acrofacial dysostosis, limbal dermoid and ocular manifestations as the keywords. Medknow Publications & Media Pvt Ltd 2014-03 /pmc/articles/PMC4061675/ /pubmed/23619496 http://dx.doi.org/10.4103/0301-4738.111194 Text en Copyright: © Indian Journal of Ophthalmology 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 | Brief Communications Malik, Rohit Goel, Sumit Aggarwal, Saurabh Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title | Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title_full | Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title_fullStr | Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title_full_unstemmed | Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title_short | Limbal dermoid in Nager acrofacial dysostosis: A rare case report |
title_sort | limbal dermoid in nager acrofacial dysostosis: a rare case report |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061675/ https://www.ncbi.nlm.nih.gov/pubmed/23619496 http://dx.doi.org/10.4103/0301-4738.111194 |
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