Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy
Type de matériel :
TexteLangue : français Détails de publication : 2019.
Sujet(s) : Ressources en ligne : Abrégé : AimsTo further characterise CDKL5-related disorder, previously classified as an early-onset seizure variant of Rett syndrome, which is currently considered a specific and independent early-infantile epileptic encephalopathy.
Nous n'avons pas d'exemplaire de ce document
32
AimsTo further characterise CDKL5-related disorder, previously classified as an early-onset seizure variant of Rett syndrome, which is currently considered a specific and independent early-infantile epileptic encephalopathy.
Réseaux sociaux