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Pediatric epilepsy syndromes with associated developmental impairment.
Nordli, Douglas R; Mclaren, John R; Araujo, Gabriel; Gupta, Megan; Nordli, Douglas R; Galan, Fernando.
Afiliação
  • Nordli DR; Department of Neurology, University of Chicago, Chicago, IL, USA.
  • Mclaren JR; Department of Pediatric Neurology, Massachusetts General Hospital, Boston, MA, USA.
  • Araujo G; Department of Pediatric Neurology, Nemours Children's Health, Jacksonville, FL, USA.
  • Gupta M; Department of Pediatrics, Children's Hospital of Los Angeles, Los Angeles, CA, USA.
  • Nordli DR; Department of Neurology, University of Chicago, Chicago, IL, USA.
  • Galan F; Department of Pediatric Neurology, Nemours Children's Health, Jacksonville, FL, USA.
Dev Med Child Neurol ; 66(6): 691-701, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38140949
ABSTRACT
In 2022, the International League Against Epilepsy revised their classification of epilepsy syndromes for clinicians to better understand the relationships between different epilepsy syndromes, their underlying causes, and their associated developmental and behavioral features. This review highlights portions of the current classification with an emphasis on epilepsy syndromes that readily present with developmental challenges and provides a unique framework, based on electroencephalography, to easily identify and understand these syndromes. Included in this review are a helpful categorization scheme with visual aid, descriptions of updated epilepsy syndromes, figures of relevant identifiers of syndrome and information regarding future directions toward treatment and research. Covered syndromes include developmental and epileptic encephalopathy, Dravet syndrome, Rasmussen syndrome, and infantile epileptic spasm syndrome, among others. WHAT THIS PAPER ADDS The revised epilepsy syndrome classification by the International League Against Epilepsy aims to improve the outcomes for children with epilepsy. The electroencephalography features of epilepsy syndromes are grouped based on a categorization model. This model allows clinicians to understand overlapping phenotypes and aid with both identification and diagnosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Síndromes Epilépticas Limite: Child / Humans Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Síndromes Epilépticas Limite: Child / Humans Idioma: En Revista: Dev Med Child Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos