Dravet syndrome with an exceptionally good seizure outcome in two adolescents

Katsuhiro Kobayashi; Iori Ohmori; Mamoru Ouchida; Yoko Ohtsuka

doi:10.1684/epd.2011.0453

Dravet syndrome with an exceptionally good seizure outcome in two adolescents

Katsuhiro Kobayashi, Iori Ohmori, Mamoru Ouchida, Yoko Ohtsuka

研究成果 › 査読

6 被引用数 (Scopus)

抄録

We present two children who exhibited the characteristics of Dravet syndrome during infancy and young childhood, with SCN1A mutation, but nevertheless achieved seizure freedom for at least four years during adolescence. These patients had no episodes of convulsive status epilepticus with a duration of more than 30 minutes and their overall favourable seizure outcome may be related to the prevention of convulsive status epilepticus.

本文言語	English
ページ（範囲）	340-344
ページ数	5
ジャーナル	Epileptic Disorders
巻	13
号	3
DOI	https://doi.org/10.1684/epd.2011.0453
出版ステータス	Published - 9月 2011

ASJC Scopus subject areas

神経学
臨床神経学

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10.1684/epd.2011.0453

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title = "Dravet syndrome with an exceptionally good seizure outcome in two adolescents",

abstract = "We present two children who exhibited the characteristics of Dravet syndrome during infancy and young childhood, with SCN1A mutation, but nevertheless achieved seizure freedom for at least four years during adolescence. These patients had no episodes of convulsive status epilepticus with a duration of more than 30 minutes and their overall favourable seizure outcome may be related to the prevention of convulsive status epilepticus.",

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AU - Ohmori, Iori

AU - Ouchida, Mamoru

AU - Ohtsuka, Yoko

PY - 2011/9

Y1 - 2011/9

N2 - We present two children who exhibited the characteristics of Dravet syndrome during infancy and young childhood, with SCN1A mutation, but nevertheless achieved seizure freedom for at least four years during adolescence. These patients had no episodes of convulsive status epilepticus with a duration of more than 30 minutes and their overall favourable seizure outcome may be related to the prevention of convulsive status epilepticus.

AB - We present two children who exhibited the characteristics of Dravet syndrome during infancy and young childhood, with SCN1A mutation, but nevertheless achieved seizure freedom for at least four years during adolescence. These patients had no episodes of convulsive status epilepticus with a duration of more than 30 minutes and their overall favourable seizure outcome may be related to the prevention of convulsive status epilepticus.

KW - Adolescence

KW - Convulsive status epilepticus

KW - Dravet syndrome

KW - Prognosis

KW - SCN1A mutation

KW - Severe myoclonic epilepsy in infancy

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Dravet syndrome with an exceptionally good seizure outcome in two adolescents

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