Severe myoclonic epilepsy in infancy (Dravet's syndrome). Some genetic aspects

The purpose of this study is to survey the data from the literature on the subject of the possible genetic origin of severe myoclonic epilepsy in infancy (SMEI). SMEI must inevitably be included within the phenotype of febrile seizures, which is made up of febrile seizures, febrile seizures plus, ge...

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Veröffentlicht in:	Revista de neurologiá 2003-07, Vol.37 (1), p.60-63
1. Verfasser:	Herranz, J L
Format:	Artikel
Sprache:	spa
Schlagworte:	Chromosomes, Human Epilepsies, Myoclonic - genetics Epilepsies, Myoclonic - metabolism Epilepsies, Myoclonic - physiopathology Humans Infant Phenotype Seizures, Febrile - metabolism Seizures, Febrile - physiopathology Sodium Channels - genetics Sodium Channels - metabolism
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