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

Research output: Contribution to journal › Review article › peer-review

6 Citations (Scopus)

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.

Original language	English
Pages (from-to)	340-344
Number of pages	5
Journal	Epileptic Disorders
Volume	13
Issue number	3
DOIs	https://doi.org/10.1684/epd.2011.0453
Publication status	Published - Sep 2011

Keywords

Adolescence
Convulsive status epilepticus
Dravet syndrome
Prognosis
SCN1A mutation
Severe myoclonic epilepsy in infancy

ASJC Scopus subject areas

Neurology
Clinical Neurology

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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.",

keywords = "Adolescence, Convulsive status epilepticus, Dravet syndrome, Prognosis, SCN1A mutation, Severe myoclonic epilepsy in infancy",

author = "Katsuhiro Kobayashi and Iori Ohmori and Mamoru Ouchida and Yoko Ohtsuka",

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AU - Kobayashi, Katsuhiro

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

Abstract

Keywords

ASJC Scopus subject areas

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