Neonatal Seizures: An Overview of Genetic Causes and Treatment Options.
benign familial neonatal epilepsy
early myoclonic encephalopathy
early-infantile epileptic encephalopathy
epilepsy
genotype-phenotype correlation
neonatal epilepsy
neonatal seizures
Journal
Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646
Informations de publication
Date de publication:
29 Sep 2021
29 Sep 2021
Historique:
received:
10
08
2021
revised:
16
09
2021
accepted:
26
09
2021
entrez:
23
10
2021
pubmed:
24
10
2021
medline:
24
10
2021
Statut:
epublish
Résumé
Seizures are the most frequent neurological clinical symptoms of the central nervous system (CNS) during the neonatal period. Neonatal seizures may be ascribed to an acute event or symptomatic conditions determined by genetic, metabolic or structural causes, outlining the so-called 'Neonatal Epilepsies'. To date, three main groups of neonatal epilepsies are recognised during the neonatal period: benign familial neonatal epilepsy (BFNE), early myoclonic encephalopathy (EME) and 'Ohtahara syndrome' (OS). Recent advances showed the role of several genes in the pathogenesis of these conditions, such as
Identifiants
pubmed: 34679360
pii: brainsci11101295
doi: 10.3390/brainsci11101295
pmc: PMC8534058
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
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