Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/54515
Title: Encefalopatías epilépticas del lactante: lo prioritario es el estudio genético [Infantile epileptic encephalopathies: what matters is genetics]
Authors: Jimenez-Legido, M
GARCÍA-PEÑAS, JUAN-JOSÉ
Filiation: Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Keywords: 
Mesh: 
Issue Date: 17-May-2017
Publisher: Viguera Editores, S. L.
Citation: Rev Neurol.2017 May;(64)s03:S65-S69
Abstract: Epileptic encephalopathies in infancy are defined as conditions where the sustained epileptic activity itself may contribute to the severe neurological and cognitive impairment. These epileptic encephalopathies include Ohtahara syndrome, early myoclonic epileptic encephalopathy, West syndrome, Dravet syndrome, and malignant migrating epilepsy in infancy. These syndromes result from identifiable primary causes, such as structural, neurodegenerative, metabolic, or genetic defects.
PMID: 28524223
URI: https://hdl.handle.net/20.500.12530/54515
Rights: info:eu-repo/semantics/openAccess
Appears in Collections:Fundaciones e Institutos de Investigación > FIB H. Infantil U. Niño Jesús > Artículos

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