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A rare case of Moebius sequence
We report a case of an 18-year-old male who presented with watering and inability to close the left eye completely since 6 months and inability to move both eyes outward and to close the mouth since childhood. Ocular, facial, and systemic examination revealed that the patient had bilateral complete...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545137/ https://www.ncbi.nlm.nih.gov/pubmed/23202399 http://dx.doi.org/10.4103/0301-4738.103798 |
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author | Kulkarni, Abhishek Madhavi, M R Nagasudha, M Bhavi, Shilpa |
author_facet | Kulkarni, Abhishek Madhavi, M R Nagasudha, M Bhavi, Shilpa |
author_sort | Kulkarni, Abhishek |
collection | PubMed |
description | We report a case of an 18-year-old male who presented with watering and inability to close the left eye completely since 6 months and inability to move both eyes outward and to close the mouth since childhood. Ocular, facial, and systemic examination revealed that the patient had bilateral complete lateral rectus and bilateral incomplete medial rectus palsy, left-sided facial nerve paralysis, thickening of lower lip and inability to close the mouth, along with other common musculoskeletal abnormalities. This is a typical presentation of Moebius syndrome which is a very rare congenital neurological disorder characterized by bilateral facial and abducens nerve paralysis. This patient had bilateral incomplete medial rectus palsy which is suggestive of the presence of horizontal gaze palsy or occulomotor nerve involvement as a component of Moebius sequence. |
format | Online Article Text |
id | pubmed-3545137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35451372013-01-16 A rare case of Moebius sequence Kulkarni, Abhishek Madhavi, M R Nagasudha, M Bhavi, Shilpa Indian J Ophthalmol Brief Communications We report a case of an 18-year-old male who presented with watering and inability to close the left eye completely since 6 months and inability to move both eyes outward and to close the mouth since childhood. Ocular, facial, and systemic examination revealed that the patient had bilateral complete lateral rectus and bilateral incomplete medial rectus palsy, left-sided facial nerve paralysis, thickening of lower lip and inability to close the mouth, along with other common musculoskeletal abnormalities. This is a typical presentation of Moebius syndrome which is a very rare congenital neurological disorder characterized by bilateral facial and abducens nerve paralysis. This patient had bilateral incomplete medial rectus palsy which is suggestive of the presence of horizontal gaze palsy or occulomotor nerve involvement as a component of Moebius sequence. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3545137/ /pubmed/23202399 http://dx.doi.org/10.4103/0301-4738.103798 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 Kulkarni, Abhishek Madhavi, M R Nagasudha, M Bhavi, Shilpa A rare case of Moebius sequence |
title | A rare case of Moebius sequence |
title_full | A rare case of Moebius sequence |
title_fullStr | A rare case of Moebius sequence |
title_full_unstemmed | A rare case of Moebius sequence |
title_short | A rare case of Moebius sequence |
title_sort | rare case of moebius sequence |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545137/ https://www.ncbi.nlm.nih.gov/pubmed/23202399 http://dx.doi.org/10.4103/0301-4738.103798 |
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