Literature DB >> 28524219

[Epileptic encephalopathies].

J Ramos-Lizana1.   

Abstract

According to the International League Against Epilepsy's (ILAE) Commission on Classification and Terminology, the term 'epileptic encephalopathy' reflects the notion that epileptic activity in itself can contribute to the genesis of severe cognitive or behavioural disabilities, beyond what could be expected from the pathology underlying the epilepsy. However, in many cases it is difficult to define the boundary between the relative contribution of the epileptic seizures and the underlying cause in the genesis of cognitive deficits. Some epileptic syndromes, such as those of West, Lennox-Gastaut or Dravet, are associated to a high probability of encephalopathic traits. The most frequent causes of epileptic encephalopathy are hypoxic-ischaemic encephalopathy, brain malformations, including cortical dysplasias, chromosomal or genetic disorders, tuberous sclerosis and metabolic diseases.

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Year:  2017        PMID: 28524219

Source DB:  PubMed          Journal:  Rev Neurol        ISSN: 0210-0010            Impact factor:   0.870


  1 in total

1.  Late-Onset Lennox-Gastaut Syndrome with Chromosome 15q Duplication in Sisters.

Authors:  Marcos Manoel Honorato; Adriane Cristina Vieira Dos Santos; Felipe Luan Lima da Silva; Renata Carvalho Cremaschi; Fernando Morgadinho Coelho
Journal:  J Neurosci Rural Pract       Date:  2022-03-08
  1 in total

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