ELECTROENCEPHALOGRAPHIC CHANGES WITH DRAVET SYNDROME

ELECTROENCEPHALOGRAPHIC CHANGES WITH DRAVET SYNDROME

Dravet syndrome (DS, severe myoclonic epilepsy of early infancy) is epileptic encephalopathy with onset in the first year of life, manifested with febrile and afebrile generalized and focal seizures, with the presence of myoclonic paroxysms in typical cases, mental retardation, and resistance to ant...

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Bibliographic Details
Main Authors: K. Yu. Mukhin, O. A. Pylaeva, M. B. Mironov, A. F. Dolinina, D. V. Morozov, M. A. Nikitina
Format: Article
Language:Russian
Published: ABV-press 2015-04-01
Series:Russkij Žurnal Detskoj Nevrologii
Subjects:
epilepsy
severe myoclonic epilepsy of early infancy
dravet syndrome
genetic basis
scn1a gene mutation
febrile seizures
myoclonic seizures
hemiclonic seizures
clinical manifestations
diagnostics
electroencephalographic characteristics
Online Access:https://rjdn.abvpress.ru/jour/article/view/34

Internet

https://rjdn.abvpress.ru/jour/article/view/34

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