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What can visual electrophysiology tell about possible visual-field defects in paediatric patients
Recognising a potential visual-field (VF) defect in paediatric patients might be challenging, especially in children before the age of 5 years and those with developmental delay or intellectual disability. Visual electrophysiological testing is an objective and non-invasive technique for evaluation...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377065/ https://www.ncbi.nlm.nih.gov/pubmed/34272512 http://dx.doi.org/10.1038/s41433-021-01680-1 |
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author | Handley, Siân E. Šuštar, Maja Tekavčič Pompe, Manca |
author_facet | Handley, Siân E. Šuštar, Maja Tekavčič Pompe, Manca |
author_sort | Handley, Siân E. |
collection | PubMed |
description | Recognising a potential visual-field (VF) defect in paediatric patients might be challenging, especially in children before the age of 5 years and those with developmental delay or intellectual disability. Visual electrophysiological testing is an objective and non-invasive technique for evaluation of visual function in paediatric patients, which can characterise the location of dysfunction and differentiate between disorders of the retina, optic nerve and visual pathway. The recording of electroretinography (ERG) and visual-evoked potentials (VEP) is possible from early days of life and requires no subjective input from the patient. As the origins of ERG and VEP tests are known, the pattern of electrophysiological changes can provide information about the VF of a child unable to perform accurate perimetry. This review summarises previously published electrophysiological findings in several common types of VF defects that can be found in paediatric patients (generalised VF defect, peripheral VF loss, central scotoma, bi-temporal hemianopia, altitudinal VF defect, quadrantanopia and homonymous hemianopia). It also shares experience on using electrophysiological testing as additional functional evidence to other tests in the clinical challenge of diagnosing or excluding VF defects in complex paediatric patients. Each type of VF defect is illustrated with one or two clinical cases. |
format | Online Article Text |
id | pubmed-8377065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83770652021-09-09 What can visual electrophysiology tell about possible visual-field defects in paediatric patients Handley, Siân E. Šuštar, Maja Tekavčič Pompe, Manca Eye (Lond) Review Article Recognising a potential visual-field (VF) defect in paediatric patients might be challenging, especially in children before the age of 5 years and those with developmental delay or intellectual disability. Visual electrophysiological testing is an objective and non-invasive technique for evaluation of visual function in paediatric patients, which can characterise the location of dysfunction and differentiate between disorders of the retina, optic nerve and visual pathway. The recording of electroretinography (ERG) and visual-evoked potentials (VEP) is possible from early days of life and requires no subjective input from the patient. As the origins of ERG and VEP tests are known, the pattern of electrophysiological changes can provide information about the VF of a child unable to perform accurate perimetry. This review summarises previously published electrophysiological findings in several common types of VF defects that can be found in paediatric patients (generalised VF defect, peripheral VF loss, central scotoma, bi-temporal hemianopia, altitudinal VF defect, quadrantanopia and homonymous hemianopia). It also shares experience on using electrophysiological testing as additional functional evidence to other tests in the clinical challenge of diagnosing or excluding VF defects in complex paediatric patients. Each type of VF defect is illustrated with one or two clinical cases. Nature Publishing Group UK 2021-07-16 2021-09 /pmc/articles/PMC8377065/ /pubmed/34272512 http://dx.doi.org/10.1038/s41433-021-01680-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Handley, Siân E. Šuštar, Maja Tekavčič Pompe, Manca What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title | What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title_full | What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title_fullStr | What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title_full_unstemmed | What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title_short | What can visual electrophysiology tell about possible visual-field defects in paediatric patients |
title_sort | what can visual electrophysiology tell about possible visual-field defects in paediatric patients |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377065/ https://www.ncbi.nlm.nih.gov/pubmed/34272512 http://dx.doi.org/10.1038/s41433-021-01680-1 |
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