Juvenile myoclonic epilepsy Epilepsia mioclônica juvenil

Juvenile myoclonus epilepsy (JME) is a common epileptic syndrome, the etiology of which is genetically determined. Its onset occurs from 6 through 22 years of age, and affected patients present with myoclonic jerks, often associated with generalized tonic-clonic seizures - the most common associatio...

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Bibliographic Details
Main Authors: Isabel Alfradique, Marcio Moacyr Vasconcelos
Format: Article
Language:English
Published: Academia Brasileira de Neurologia (ABNEURO) 2007-12-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2007000700036