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Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis

Isolated unilateral congenital ptosis is encountered relatively infrequently in clinical practice. It typically consists of a unilateral droopy eyelid, weak levator palpebrae superioris muscle function, lid lag, and an absent upper lid crease with no other abnormalities on examination. We present a...

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Autores principales: Salman, Michael S., Clark, Ian H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418841/
https://www.ncbi.nlm.nih.gov/pubmed/28529498
http://dx.doi.org/10.3389/fneur.2017.00190
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author Salman, Michael S.
Clark, Ian H.
author_facet Salman, Michael S.
Clark, Ian H.
author_sort Salman, Michael S.
collection PubMed
description Isolated unilateral congenital ptosis is encountered relatively infrequently in clinical practice. It typically consists of a unilateral droopy eyelid, weak levator palpebrae superioris muscle function, lid lag, and an absent upper lid crease with no other abnormalities on examination. We present a four-and-a-half-year-old girl with isolated and mild unilateral congenital ptosis who unexpectedly demonstrated a static upper eyelid on downgaze in conjunction with a well-formed upper lid skin crease. We attribute this uncommon sign in congenital ptosis to stiffness and presumed fibrosis of the levator muscle. Examining the function of the eyelids in all directions of gaze is important in patients with abnormalities of lid position, since additional useful information can be gleaned about the status of the levator muscle including, aberrant regeneration or fibrosis.
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spelling pubmed-54188412017-05-19 Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis Salman, Michael S. Clark, Ian H. Front Neurol Neuroscience Isolated unilateral congenital ptosis is encountered relatively infrequently in clinical practice. It typically consists of a unilateral droopy eyelid, weak levator palpebrae superioris muscle function, lid lag, and an absent upper lid crease with no other abnormalities on examination. We present a four-and-a-half-year-old girl with isolated and mild unilateral congenital ptosis who unexpectedly demonstrated a static upper eyelid on downgaze in conjunction with a well-formed upper lid skin crease. We attribute this uncommon sign in congenital ptosis to stiffness and presumed fibrosis of the levator muscle. Examining the function of the eyelids in all directions of gaze is important in patients with abnormalities of lid position, since additional useful information can be gleaned about the status of the levator muscle including, aberrant regeneration or fibrosis. Frontiers Media S.A. 2017-05-05 /pmc/articles/PMC5418841/ /pubmed/28529498 http://dx.doi.org/10.3389/fneur.2017.00190 Text en Copyright © 2017 Salman and Clark. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Salman, Michael S.
Clark, Ian H.
Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title_full Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title_fullStr Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title_full_unstemmed Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title_short Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis
title_sort eyelid retraction in isolated unilateral congenital blepharoptosis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418841/
https://www.ncbi.nlm.nih.gov/pubmed/28529498
http://dx.doi.org/10.3389/fneur.2017.00190
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