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Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction

INTRODUCTION: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral palsies of the cranial nerves VI and VII, resulting in congenital facial paralysis sometimes associated with impaired ocular abduction. CASE REPORT: We present the case of a 44-year-old woman with Möbius...

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Autores principales: Lopez-Valverde, Gloria, Jarrin-Hernandez, Elena, Cruz-Gonzalez, Fernando, Mateos-Sanchez, Encarnacion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843936/
https://www.ncbi.nlm.nih.gov/pubmed/24348407
http://dx.doi.org/10.1159/000356528
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author Lopez-Valverde, Gloria
Jarrin-Hernandez, Elena
Cruz-Gonzalez, Fernando
Mateos-Sanchez, Encarnacion
author_facet Lopez-Valverde, Gloria
Jarrin-Hernandez, Elena
Cruz-Gonzalez, Fernando
Mateos-Sanchez, Encarnacion
author_sort Lopez-Valverde, Gloria
collection PubMed
description INTRODUCTION: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral palsies of the cranial nerves VI and VII, resulting in congenital facial paralysis sometimes associated with impaired ocular abduction. CASE REPORT: We present the case of a 44-year-old woman with Möbius syndrome and inferior recurrent keratitis secondary to scleral show in both eyes. We decided to use a cartilage graft from the ear in the inferior eyelid to avoid eyelid retraction and scleral show. DISCUSSION: Patients with Möbius syndrome have a severe dysfunction of their facial mimic. Their treatment must be individualized, depending on their age, clinical examination and symptoms.
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spelling pubmed-38439362013-12-12 Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction Lopez-Valverde, Gloria Jarrin-Hernandez, Elena Cruz-Gonzalez, Fernando Mateos-Sanchez, Encarnacion Case Rep Ophthalmol Published online: November, 2013 INTRODUCTION: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral palsies of the cranial nerves VI and VII, resulting in congenital facial paralysis sometimes associated with impaired ocular abduction. CASE REPORT: We present the case of a 44-year-old woman with Möbius syndrome and inferior recurrent keratitis secondary to scleral show in both eyes. We decided to use a cartilage graft from the ear in the inferior eyelid to avoid eyelid retraction and scleral show. DISCUSSION: Patients with Möbius syndrome have a severe dysfunction of their facial mimic. Their treatment must be individualized, depending on their age, clinical examination and symptoms. S. Karger AG 2013-11-05 /pmc/articles/PMC3843936/ /pubmed/24348407 http://dx.doi.org/10.1159/000356528 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: November, 2013
Lopez-Valverde, Gloria
Jarrin-Hernandez, Elena
Cruz-Gonzalez, Fernando
Mateos-Sanchez, Encarnacion
Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title_full Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title_fullStr Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title_full_unstemmed Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title_short Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction
title_sort möbius syndrome: surgical treatment for eyelid dysfunction
topic Published online: November, 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843936/
https://www.ncbi.nlm.nih.gov/pubmed/24348407
http://dx.doi.org/10.1159/000356528
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