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Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate

Alice in Wonderland syndrome is a disorienting perceptual disorder characterized by discrete episodes of bizarre visual illusions and spatial distortions which has been associated with numerous neurologic and psychiatric conditions. Little is known regarding the electrophysiologic correlates of the...

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Detalles Bibliográficos
Autores principales: Shah, Arya, Magaña, Setty M., E. Youssef, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294370/
https://www.ncbi.nlm.nih.gov/pubmed/32587880
http://dx.doi.org/10.1177/2329048X20932714
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author Shah, Arya
Magaña, Setty M.
E. Youssef, Paul
author_facet Shah, Arya
Magaña, Setty M.
E. Youssef, Paul
author_sort Shah, Arya
collection PubMed
description Alice in Wonderland syndrome is a disorienting perceptual disorder characterized by discrete episodes of bizarre visual illusions and spatial distortions which has been associated with numerous neurologic and psychiatric conditions. Little is known regarding the electrophysiologic correlates of the visual symptoms described in this syndrome. The authors report the unique case of an 8-year-old boy presenting with visual distortions consistent with Alice in Wonderland syndrome, and an electroencephalogram demonstrating bilateral temporo-occipital slowing which correlated with symptoms of micropsia, teleopsia, and dysmorphopsia. Identification of this clinical syndrome and its electroclinical features are important for establishing a proper diagnosis and subsequent reassurance or appropriate treatment directed toward the underlying etiology.
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spelling pubmed-72943702020-06-24 Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate Shah, Arya Magaña, Setty M. E. Youssef, Paul Child Neurol Open Case Report Alice in Wonderland syndrome is a disorienting perceptual disorder characterized by discrete episodes of bizarre visual illusions and spatial distortions which has been associated with numerous neurologic and psychiatric conditions. Little is known regarding the electrophysiologic correlates of the visual symptoms described in this syndrome. The authors report the unique case of an 8-year-old boy presenting with visual distortions consistent with Alice in Wonderland syndrome, and an electroencephalogram demonstrating bilateral temporo-occipital slowing which correlated with symptoms of micropsia, teleopsia, and dysmorphopsia. Identification of this clinical syndrome and its electroclinical features are important for establishing a proper diagnosis and subsequent reassurance or appropriate treatment directed toward the underlying etiology. SAGE Publications 2020-06-12 /pmc/articles/PMC7294370/ /pubmed/32587880 http://dx.doi.org/10.1177/2329048X20932714 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Shah, Arya
Magaña, Setty M.
E. Youssef, Paul
Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title_full Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title_fullStr Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title_full_unstemmed Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title_short Do You See What I See? A Case of Alice in Wonderland Syndrome With EEG Correlate
title_sort do you see what i see? a case of alice in wonderland syndrome with eeg correlate
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294370/
https://www.ncbi.nlm.nih.gov/pubmed/32587880
http://dx.doi.org/10.1177/2329048X20932714
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