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Horner syndrome: clinical perspectives
Horner syndrome consists of unilateral ptosis, an ipsilateral miotic but normally reactive pupil, and in some cases, ipsilateral facial anhidrosis, all resulting from damage to the ipsilateral oculosympathetic pathway. Herein, we review the clinical signs and symptoms that can aid in the diagnosis a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398733/ https://www.ncbi.nlm.nih.gov/pubmed/28539793 http://dx.doi.org/10.2147/EB.S63633 |
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author | Kanagalingam, Sivashakthi Miller, Neil R |
author_facet | Kanagalingam, Sivashakthi Miller, Neil R |
author_sort | Kanagalingam, Sivashakthi |
collection | PubMed |
description | Horner syndrome consists of unilateral ptosis, an ipsilateral miotic but normally reactive pupil, and in some cases, ipsilateral facial anhidrosis, all resulting from damage to the ipsilateral oculosympathetic pathway. Herein, we review the clinical signs and symptoms that can aid in the diagnosis and localization of a Horner syndrome as well as the causes of the condition. We emphasize that pharmacologic testing can confirm its presence and direct further testing and management. |
format | Online Article Text |
id | pubmed-5398733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53987332017-05-24 Horner syndrome: clinical perspectives Kanagalingam, Sivashakthi Miller, Neil R Eye Brain Review Horner syndrome consists of unilateral ptosis, an ipsilateral miotic but normally reactive pupil, and in some cases, ipsilateral facial anhidrosis, all resulting from damage to the ipsilateral oculosympathetic pathway. Herein, we review the clinical signs and symptoms that can aid in the diagnosis and localization of a Horner syndrome as well as the causes of the condition. We emphasize that pharmacologic testing can confirm its presence and direct further testing and management. Dove Medical Press 2015-04-10 /pmc/articles/PMC5398733/ /pubmed/28539793 http://dx.doi.org/10.2147/EB.S63633 Text en © 2015 Kanagalingam and Miller. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Kanagalingam, Sivashakthi Miller, Neil R Horner syndrome: clinical perspectives |
title | Horner syndrome: clinical perspectives |
title_full | Horner syndrome: clinical perspectives |
title_fullStr | Horner syndrome: clinical perspectives |
title_full_unstemmed | Horner syndrome: clinical perspectives |
title_short | Horner syndrome: clinical perspectives |
title_sort | horner syndrome: clinical perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398733/ https://www.ncbi.nlm.nih.gov/pubmed/28539793 http://dx.doi.org/10.2147/EB.S63633 |
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