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Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation
We report a case of Wildervanck syndrome exhibiting Klippel–Feil anomaly, Duane's retraction syndrome and congenital deafness. Since the first case was reported in 1952, there have been more reports describing this triad either complete or incomplete. Our case has a complete triad of the syndro...
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/PMC4228573/ https://www.ncbi.nlm.nih.gov/pubmed/25400350 http://dx.doi.org/10.4103/0971-6866.142899 |
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author | Meshram, Suwansh Sukhadeorao Nikose, Sheetal Jain, Shraddha Taksande, Amar |
author_facet | Meshram, Suwansh Sukhadeorao Nikose, Sheetal Jain, Shraddha Taksande, Amar |
author_sort | Meshram, Suwansh Sukhadeorao |
collection | PubMed |
description | We report a case of Wildervanck syndrome exhibiting Klippel–Feil anomaly, Duane's retraction syndrome and congenital deafness. Since the first case was reported in 1952, there have been more reports describing this triad either complete or incomplete. Our case has a complete triad of the syndrome along with frontal sinus hypoplasia. Our case is unique as the triad was associated with frontal sinus hypoplasia, which is very rare association. |
format | Online Article Text |
id | pubmed-4228573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42285732014-11-14 Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation Meshram, Suwansh Sukhadeorao Nikose, Sheetal Jain, Shraddha Taksande, Amar Indian J Hum Genet Case Report We report a case of Wildervanck syndrome exhibiting Klippel–Feil anomaly, Duane's retraction syndrome and congenital deafness. Since the first case was reported in 1952, there have been more reports describing this triad either complete or incomplete. Our case has a complete triad of the syndrome along with frontal sinus hypoplasia. Our case is unique as the triad was associated with frontal sinus hypoplasia, which is very rare association. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4228573/ /pubmed/25400350 http://dx.doi.org/10.4103/0971-6866.142899 Text en Copyright: © Indian Journal of Human Genetics 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 Meshram, Suwansh Sukhadeorao Nikose, Sheetal Jain, Shraddha Taksande, Amar Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title | Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title_full | Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title_fullStr | Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title_full_unstemmed | Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title_short | Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation |
title_sort | wildervanck syndrome with hypoplastic frontal sinus: a rare case presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228573/ https://www.ncbi.nlm.nih.gov/pubmed/25400350 http://dx.doi.org/10.4103/0971-6866.142899 |
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