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Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy

Panayiotopoulos syndrome (PS) is a self-limited focal epilepsy appearing in childhood. Seizures in PS are self-limiting and do not usually continue into adulthood. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized epilepsy, developing around puberty and continuing t...

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Autores principales: Enoki, Hideo, Itamura, Shinji, Baba, Shimpei, Okanishi, Tohru, Fujimoto, Ayataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744758/
https://www.ncbi.nlm.nih.gov/pubmed/33343495
http://dx.doi.org/10.3389/fneur.2020.591477
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author Enoki, Hideo
Itamura, Shinji
Baba, Shimpei
Okanishi, Tohru
Fujimoto, Ayataka
author_facet Enoki, Hideo
Itamura, Shinji
Baba, Shimpei
Okanishi, Tohru
Fujimoto, Ayataka
author_sort Enoki, Hideo
collection PubMed
description Panayiotopoulos syndrome (PS) is a self-limited focal epilepsy appearing in childhood. Seizures in PS are self-limiting and do not usually continue into adulthood. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized epilepsy, developing around puberty and continuing throughout adulthood. We describe four cases of PS in childhood in which JME developed in adolescence. Age at onset ranged from 4 to 8 years for PS, and 11 to 14 years for JME. JME developed after PS subsided, with the interval between last PS seizure and first JME seizure ranging from 1 to 10 years. No link between the two conditions has previously been described. Since PS is considered to show good prognosis and to be self-limiting, long-term observation has been considered unnecessary. No definitive factors were found to predict future evolution to JME in our series, so longer-term follow-up may be warranted for all PS patients.
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spelling pubmed-77447582020-12-18 Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy Enoki, Hideo Itamura, Shinji Baba, Shimpei Okanishi, Tohru Fujimoto, Ayataka Front Neurol Neurology Panayiotopoulos syndrome (PS) is a self-limited focal epilepsy appearing in childhood. Seizures in PS are self-limiting and do not usually continue into adulthood. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized epilepsy, developing around puberty and continuing throughout adulthood. We describe four cases of PS in childhood in which JME developed in adolescence. Age at onset ranged from 4 to 8 years for PS, and 11 to 14 years for JME. JME developed after PS subsided, with the interval between last PS seizure and first JME seizure ranging from 1 to 10 years. No link between the two conditions has previously been described. Since PS is considered to show good prognosis and to be self-limiting, long-term observation has been considered unnecessary. No definitive factors were found to predict future evolution to JME in our series, so longer-term follow-up may be warranted for all PS patients. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7744758/ /pubmed/33343495 http://dx.doi.org/10.3389/fneur.2020.591477 Text en Copyright © 2020 Enoki, Itamura, Baba, Okanishi and Fujimoto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Enoki, Hideo
Itamura, Shinji
Baba, Shimpei
Okanishi, Tohru
Fujimoto, Ayataka
Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title_full Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title_fullStr Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title_full_unstemmed Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title_short Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy
title_sort case report: four cases of panayiotopoulos syndrome evolving to juvenile myoclonic epilepsy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744758/
https://www.ncbi.nlm.nih.gov/pubmed/33343495
http://dx.doi.org/10.3389/fneur.2020.591477
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