Skip to Main Content (Press Enter)

Logo CNR
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Strutture
  • Competenze

UNI-FIND
Logo CNR

|

UNI-FIND

cnr.it
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Strutture
  • Competenze
  1. Pubblicazioni

Genetics of epilepsy and relevance to current practice

Articolo
Data di Pubblicazione:
2012
Abstract:
Genetic factors are likely to play a major role in many epileptic conditions, spanning from classical idiopathic (genetic) generalized epilepsies to epileptic encephalopathies and focal epilepsies. In this review we describe the genetic advances in progressive myoclonus epilepsies, which are strictly monogenic disorders, genetic generalized epilepsies, mostly exhibiting complex genetic inheritance, and SCN1A-related phenotypes, namely genetic generalized epilepsy with febrile seizure plus and Dravet syndrome. Particular attention is devoted to a form of familial focal epilepsies, autosomaldominant lateral temporal epilepsy, which is a model of non-ion genetic epilepsies. This condition is associated with mutations of the LGI1 gene, whose protein is secreted from the neurons and exerts its action on a number of targets, influencing cortical development and neuronal maturation. © Springer Science+Business Media, LLC 2012.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Autosomal-dominant lateral temporal epilepsy; Dravet syndrome; Genetic epilepsies; LGI1 mutations; Progressive myoclonus epilepsies; SCN1A-related phenotypes
Elenco autori:
Nobile, Carlo
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/279181
Pubblicato in:
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS
Journal
  • Dati Generali

Dati Generali

URL

http://www.scopus.com/record/display.url?eid=2-s2.0-84876904325&origin=inward
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.0.0 | Sorgente dati: PREPROD (Ribaltamento disabilitato)