Gastaut type idiopathic childhood occipital epilepsy

Detalhes bibliográficos
Autor(a) principal: Ferrari-Marinho, Taissa [UNIFESP]
Data de Publicação: 2013
Outros Autores: Macedo, Eugenia Fialho [UNIFESP], Neves, Rafael Scarpa da Costa [UNIFESP], Costa, Livia Vianez [UNIFESP], Tudesco, Ivanda de Souza Silva [UNIFESP], Carvalho, Kelly C. [UNIFESP], Carrete, Henrique [UNIFESP], Caboclo, Luis Otávio [UNIFESP], Yacubian, Elza Márcia Targas [UNIFESP], Hamad, Ana Paula [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1684/epd.2013.0551
http://repositorio.unifesp.br/handle/11600/36010
Resumo: Gastaut type idiopathic childhood occipital epilepsy is an uncommon epileptic syndrome characterised by frequent seizures, most commonly presenting as elementary visual hallucinations or blindness. Other occipital (non-visual) symptoms may also occur. Interictal EEG typically shows occipital paroxysms, often with fixation-off sensitivity. Ictal EEG is usually characterised by interruption by paroxysms and sudden appearance of low-voltage, occipital, fast rhythm and/or spikes. Despite well described clinical and EEG patterns, to our knowledge, there are very few reports in the literature with video-EEG recording of either seizure semiology or fixation-off phenomena. We present a video-EEG recording of a 12-year-old girl with Gastaut type epilepsy, illustrating the interictal and ictal aspects of this syndrome. Our aim was to demonstrate the clinical and neurophysiological pattern of a typical seizure of Gastaut type epilepsy, as well as the fixation-off phenomena, in order to further clarify the typical presentation of this syndrome. [Published with video sequences]
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spelling Gastaut type idiopathic childhood occipital epilepsyidiopathic childhood epilepsyGastaut type epilepsyvideo-EEGGastaut type idiopathic childhood occipital epilepsy is an uncommon epileptic syndrome characterised by frequent seizures, most commonly presenting as elementary visual hallucinations or blindness. Other occipital (non-visual) symptoms may also occur. Interictal EEG typically shows occipital paroxysms, often with fixation-off sensitivity. Ictal EEG is usually characterised by interruption by paroxysms and sudden appearance of low-voltage, occipital, fast rhythm and/or spikes. Despite well described clinical and EEG patterns, to our knowledge, there are very few reports in the literature with video-EEG recording of either seizure semiology or fixation-off phenomena. We present a video-EEG recording of a 12-year-old girl with Gastaut type epilepsy, illustrating the interictal and ictal aspects of this syndrome. Our aim was to demonstrate the clinical and neurophysiological pattern of a typical seizure of Gastaut type epilepsy, as well as the fixation-off phenomena, in order to further clarify the typical presentation of this syndrome. [Published with video sequences]Universidade Federal de São Paulo, Hosp São Paulo, Dept Neurol & Neurosurg, BR-04024002 São Paulo, BrazilUniversidade Federal de São Paulo, Hosp São Paulo, Dept Imaging Diag, BR-04024002 São Paulo, BrazilUniversidade Federal de São Paulo, Hosp São Paulo, Dept Neurol & Neurosurg, BR-04024002 São Paulo, BrazilUniversidade Federal de São Paulo, Hosp São Paulo, Dept Imaging Diag, BR-04024002 São Paulo, BrazilWeb of ScienceJohn Libbey Eurotext LtdUniversidade Federal de São Paulo (UNIFESP)Ferrari-Marinho, Taissa [UNIFESP]Macedo, Eugenia Fialho [UNIFESP]Neves, Rafael Scarpa da Costa [UNIFESP]Costa, Livia Vianez [UNIFESP]Tudesco, Ivanda de Souza Silva [UNIFESP]Carvalho, Kelly C. [UNIFESP]Carrete, Henrique [UNIFESP]Caboclo, Luis Otávio [UNIFESP]Yacubian, Elza Márcia Targas [UNIFESP]Hamad, Ana Paula [UNIFESP]2016-01-24T14:31:18Z2016-01-24T14:31:18Z2013-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion80-83http://dx.doi.org/10.1684/epd.2013.0551Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 15, n. 1, p. 80-83, 2013.10.1684/epd.2013.05511294-9361http://repositorio.unifesp.br/handle/11600/36010WOS:000317594400013engEpileptic Disordersinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-02-15T11:04:56Zoai:repositorio.unifesp.br/:11600/36010Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-02-15T11:04:56Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Gastaut type idiopathic childhood occipital epilepsy
title Gastaut type idiopathic childhood occipital epilepsy
spellingShingle Gastaut type idiopathic childhood occipital epilepsy
Ferrari-Marinho, Taissa [UNIFESP]
idiopathic childhood epilepsy
Gastaut type epilepsy
video-EEG
title_short Gastaut type idiopathic childhood occipital epilepsy
title_full Gastaut type idiopathic childhood occipital epilepsy
title_fullStr Gastaut type idiopathic childhood occipital epilepsy
title_full_unstemmed Gastaut type idiopathic childhood occipital epilepsy
title_sort Gastaut type idiopathic childhood occipital epilepsy
author Ferrari-Marinho, Taissa [UNIFESP]
author_facet Ferrari-Marinho, Taissa [UNIFESP]
Macedo, Eugenia Fialho [UNIFESP]
Neves, Rafael Scarpa da Costa [UNIFESP]
Costa, Livia Vianez [UNIFESP]
Tudesco, Ivanda de Souza Silva [UNIFESP]
Carvalho, Kelly C. [UNIFESP]
Carrete, Henrique [UNIFESP]
Caboclo, Luis Otávio [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
Hamad, Ana Paula [UNIFESP]
author_role author
author2 Macedo, Eugenia Fialho [UNIFESP]
Neves, Rafael Scarpa da Costa [UNIFESP]
Costa, Livia Vianez [UNIFESP]
Tudesco, Ivanda de Souza Silva [UNIFESP]
Carvalho, Kelly C. [UNIFESP]
Carrete, Henrique [UNIFESP]
Caboclo, Luis Otávio [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
Hamad, Ana Paula [UNIFESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ferrari-Marinho, Taissa [UNIFESP]
Macedo, Eugenia Fialho [UNIFESP]
Neves, Rafael Scarpa da Costa [UNIFESP]
Costa, Livia Vianez [UNIFESP]
Tudesco, Ivanda de Souza Silva [UNIFESP]
Carvalho, Kelly C. [UNIFESP]
Carrete, Henrique [UNIFESP]
Caboclo, Luis Otávio [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
Hamad, Ana Paula [UNIFESP]
dc.subject.por.fl_str_mv idiopathic childhood epilepsy
Gastaut type epilepsy
video-EEG
topic idiopathic childhood epilepsy
Gastaut type epilepsy
video-EEG
description Gastaut type idiopathic childhood occipital epilepsy is an uncommon epileptic syndrome characterised by frequent seizures, most commonly presenting as elementary visual hallucinations or blindness. Other occipital (non-visual) symptoms may also occur. Interictal EEG typically shows occipital paroxysms, often with fixation-off sensitivity. Ictal EEG is usually characterised by interruption by paroxysms and sudden appearance of low-voltage, occipital, fast rhythm and/or spikes. Despite well described clinical and EEG patterns, to our knowledge, there are very few reports in the literature with video-EEG recording of either seizure semiology or fixation-off phenomena. We present a video-EEG recording of a 12-year-old girl with Gastaut type epilepsy, illustrating the interictal and ictal aspects of this syndrome. Our aim was to demonstrate the clinical and neurophysiological pattern of a typical seizure of Gastaut type epilepsy, as well as the fixation-off phenomena, in order to further clarify the typical presentation of this syndrome. [Published with video sequences]
publishDate 2013
dc.date.none.fl_str_mv 2013-03-01
2016-01-24T14:31:18Z
2016-01-24T14:31:18Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1684/epd.2013.0551
Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 15, n. 1, p. 80-83, 2013.
10.1684/epd.2013.0551
1294-9361
http://repositorio.unifesp.br/handle/11600/36010
WOS:000317594400013
url http://dx.doi.org/10.1684/epd.2013.0551
http://repositorio.unifesp.br/handle/11600/36010
identifier_str_mv Epileptic Disorders. Montrouge: John Libbey Eurotext Ltd, v. 15, n. 1, p. 80-83, 2013.
10.1684/epd.2013.0551
1294-9361
WOS:000317594400013
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Epileptic Disorders
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 80-83
dc.publisher.none.fl_str_mv John Libbey Eurotext Ltd
publisher.none.fl_str_mv John Libbey Eurotext Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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