Horner syndrome: clinical perspectives
Sivashakthi Kanagalingam,1–3 Neil R Miller1–31Department of Ophthalmology, 2Department of Neurology, 3Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, MD, USAAbstract: Horner syndrome consists of unilateral ptosis, an ipsilateral miotic but normally reactive pu...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2015-04-01
|
Series: | Eye and Brain |
Online Access: | http://www.dovepress.com/horner-syndrome-clinical-perspectives-peer-reviewed-article-EB |
id |
doaj-e20c92c1dce1448d9ce1028e2679bfdb |
---|---|
record_format |
Article |
spelling |
doaj-e20c92c1dce1448d9ce1028e2679bfdb2020-11-24T21:05:32ZengDove Medical PressEye and Brain1179-27442015-04-012015default354621276Horner syndrome: clinical perspectivesKanagalingam SMiller NR Sivashakthi Kanagalingam,1–3 Neil R Miller1–31Department of Ophthalmology, 2Department of Neurology, 3Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, MD, USAAbstract: 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.Keywords: Horner syndrome, oculosympathoparesis, anisocoria, ptosis, anhidrosishttp://www.dovepress.com/horner-syndrome-clinical-perspectives-peer-reviewed-article-EB |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kanagalingam S Miller NR |
spellingShingle |
Kanagalingam S Miller NR Horner syndrome: clinical perspectives Eye and Brain |
author_facet |
Kanagalingam S Miller NR |
author_sort |
Kanagalingam S |
title |
Horner syndrome: clinical perspectives |
title_short |
Horner syndrome: clinical perspectives |
title_full |
Horner syndrome: clinical perspectives |
title_fullStr |
Horner syndrome: clinical perspectives |
title_full_unstemmed |
Horner syndrome: clinical perspectives |
title_sort |
horner syndrome: clinical perspectives |
publisher |
Dove Medical Press |
series |
Eye and Brain |
issn |
1179-2744 |
publishDate |
2015-04-01 |
description |
Sivashakthi Kanagalingam,1–3 Neil R Miller1–31Department of Ophthalmology, 2Department of Neurology, 3Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, MD, USAAbstract: 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.Keywords: Horner syndrome, oculosympathoparesis, anisocoria, ptosis, anhidrosis |
url |
http://www.dovepress.com/horner-syndrome-clinical-perspectives-peer-reviewed-article-EB |
work_keys_str_mv |
AT kanagalingams hornersyndromeclinicalperspectives AT millernr hornersyndromeclinicalperspectives |
_version_ |
1716768400824336384 |