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Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report

Juvenile myoclonic epilepsy (JME) has well-defined clinical and electrophysiological features. On the other hand, large case series have shown that focal and asymmetrical discharges may accompany generalized epileptiform activities in JME. Although it is known that these non-generalized electrophysi...

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Autores principales: Suzgun, Merve Aktan, Demirbilek, Veysi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830026/
https://www.ncbi.nlm.nih.gov/pubmed/36685744
http://dx.doi.org/10.14581/jer.22014
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author Suzgun, Merve Aktan
Demirbilek, Veysi
author_facet Suzgun, Merve Aktan
Demirbilek, Veysi
author_sort Suzgun, Merve Aktan
collection PubMed
description Juvenile myoclonic epilepsy (JME) has well-defined clinical and electrophysiological features. On the other hand, large case series have shown that focal and asymmetrical discharges may accompany generalized epileptiform activities in JME. Although it is known that these non-generalized electrophysiological findings do not exclude the diagnosis of this syndrome, some findings may create confusion in the differential diagnosis. In this case report, a case of JME with electroencephalographic findings characterized by isolated unilateral epileptiform activities without typical generalized discharges was discussed. The current case clinically presented with involuntary jerk movements in the bilateral upper extremities. It has been determined that these movements are uni/bilateral myoclonic beats based on home video recordings. Metabolic, toxic and structural problems were excluded in the investigations for the etiology of myoclonus. In the electrophysiological examination performed for epileptic processes, epileptiform discharges localized to the isolated right hemisphere were observed. JME was considered primarily due to clinical findings in the patient, and effective seizure control was achieved in a 4-year follow-up under anti-seizure treatment. The peculiarity of the case is the presence of electrophysiology recordings of isolated unilateral epileptiform activity during the 4-year follow-up period. It should be emphasized that there is no case of JME diagnosed with isolated unilateral epileptiform activity in the absence of generalized spike-slow waves or multiple spike-slow waves in the literature.
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spelling pubmed-98300262023-01-19 Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report Suzgun, Merve Aktan Demirbilek, Veysi J Epilepsy Res Case Report Juvenile myoclonic epilepsy (JME) has well-defined clinical and electrophysiological features. On the other hand, large case series have shown that focal and asymmetrical discharges may accompany generalized epileptiform activities in JME. Although it is known that these non-generalized electrophysiological findings do not exclude the diagnosis of this syndrome, some findings may create confusion in the differential diagnosis. In this case report, a case of JME with electroencephalographic findings characterized by isolated unilateral epileptiform activities without typical generalized discharges was discussed. The current case clinically presented with involuntary jerk movements in the bilateral upper extremities. It has been determined that these movements are uni/bilateral myoclonic beats based on home video recordings. Metabolic, toxic and structural problems were excluded in the investigations for the etiology of myoclonus. In the electrophysiological examination performed for epileptic processes, epileptiform discharges localized to the isolated right hemisphere were observed. JME was considered primarily due to clinical findings in the patient, and effective seizure control was achieved in a 4-year follow-up under anti-seizure treatment. The peculiarity of the case is the presence of electrophysiology recordings of isolated unilateral epileptiform activity during the 4-year follow-up period. It should be emphasized that there is no case of JME diagnosed with isolated unilateral epileptiform activity in the absence of generalized spike-slow waves or multiple spike-slow waves in the literature. Korean Epilepsy Society 2022-12-30 /pmc/articles/PMC9830026/ /pubmed/36685744 http://dx.doi.org/10.14581/jer.22014 Text en Copyright © 2022 Korean Epilepsy Society https://creativecommons.org/licenses/by-nc/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Suzgun, Merve Aktan
Demirbilek, Veysi
Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title_full Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title_fullStr Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title_full_unstemmed Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title_short Isolated Unilateral EEG Findings in Juvenile Myoclonic Epilepsy: A Case Report
title_sort isolated unilateral eeg findings in juvenile myoclonic epilepsy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830026/
https://www.ncbi.nlm.nih.gov/pubmed/36685744
http://dx.doi.org/10.14581/jer.22014
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