Recent developments in the genetics of childhood epileptic encephalopathies: impact in clinical practice

• Autor(a) principal: Gonsales,Marina C.
• Data de Publicação: 2015
• Outros Autores: Montenegro,Maria Augusta, Soler,Camila V., Coan,Ana Carolina, Guerreiro,Marilisa M., Lopes-Cendes,Iscia
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Arquivos de neuro-psiquiatria (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2015001100946
• topic: Dravet syndrome; Ohtahara syndrome; West syndrome; Lennox-Gastaut syndrome; Doose syndrome; Landau-Kleffner syndrome

Recent advances in molecular genetics led to the discovery of several genes for childhood epileptic encephalopathies (CEEs). As the knowledge about the genes associated with this group of disorders develops, it becomes evident that CEEs present a number of specific genetic characteristics, which will influence the use of molecular testing for clinical purposes. Among these, there are the presence of marked genetic heterogeneity and the high frequency of de novo mutations. Therefore, the main objectives of this review paper are to present and discuss current knowledge regarding i) new genetic findings in CEEs, ii) phenotype-genotype correlations in different forms of CEEs; and, most importantly, iii) the impact of these new findings in clinical practice. Accompanying this text we have included a comprehensive table, containing the list of genes currently known to be involved in the etiology of CEEs.