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Total levator aponeurosis resection for primary congenital ptosis with very poor levator function

AIM: This study was designed to evaluate the effectiveness of total levator aponeurosis resection in patients with very poor levator function secondary to primary congenital ptosis. DESIGN: A retrospective, noncomparative single-institutional study was designed. PARTICIPANTS: Seven patients with ver...

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Detalles Bibliográficos
Autores principales: Al-Mujaini, Abdullah, Wali, Upender K.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992158/
https://www.ncbi.nlm.nih.gov/pubmed/21120047
http://dx.doi.org/10.4103/0974-620X.71886
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author Al-Mujaini, Abdullah
Wali, Upender K.
author_facet Al-Mujaini, Abdullah
Wali, Upender K.
author_sort Al-Mujaini, Abdullah
collection PubMed
description AIM: This study was designed to evaluate the effectiveness of total levator aponeurosis resection in patients with very poor levator function secondary to primary congenital ptosis. DESIGN: A retrospective, noncomparative single-institutional study was designed. PARTICIPANTS: Seven patients with very poor levator function secondary to primary congenital ptosis operated between May 2008 and May 2010 by one surgeon (AM). MATERIALS AND METHODS: A retrospective study of seven patients with congenital ptosis evaluating eyelid elevation following total levator aponeurosis resection. End result is improvement of the eyelid elevation. CONCLUSION: Total levator aponeurosis resection is easy and effective tool in elevating the eyelid in patients with very poor levator function secondary to primary congenital ptosis.
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spelling pubmed-29921582010-11-30 Total levator aponeurosis resection for primary congenital ptosis with very poor levator function Al-Mujaini, Abdullah Wali, Upender K. Oman J Ophthalmol Original Article AIM: This study was designed to evaluate the effectiveness of total levator aponeurosis resection in patients with very poor levator function secondary to primary congenital ptosis. DESIGN: A retrospective, noncomparative single-institutional study was designed. PARTICIPANTS: Seven patients with very poor levator function secondary to primary congenital ptosis operated between May 2008 and May 2010 by one surgeon (AM). MATERIALS AND METHODS: A retrospective study of seven patients with congenital ptosis evaluating eyelid elevation following total levator aponeurosis resection. End result is improvement of the eyelid elevation. CONCLUSION: Total levator aponeurosis resection is easy and effective tool in elevating the eyelid in patients with very poor levator function secondary to primary congenital ptosis. Medknow Publications 2010 /pmc/articles/PMC2992158/ /pubmed/21120047 http://dx.doi.org/10.4103/0974-620X.71886 Text en © Oman Journal of Ophthalmology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Al-Mujaini, Abdullah
Wali, Upender K.
Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title_full Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title_fullStr Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title_full_unstemmed Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title_short Total levator aponeurosis resection for primary congenital ptosis with very poor levator function
title_sort total levator aponeurosis resection for primary congenital ptosis with very poor levator function
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992158/
https://www.ncbi.nlm.nih.gov/pubmed/21120047
http://dx.doi.org/10.4103/0974-620X.71886
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