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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...

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Autores principales: Malik, Rohit, Goel, Sumit, Aggarwal, Saurabh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
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.
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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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