Treatment of infantile spasms: why do we know so little?
ACTH
Infantile spasms
animal models
epileptic spasms
malformation of cortical development
outcome
prednisone
treatment
tuberous sclerosis complex
vigabatrin
Journal
Expert review of neurotherapeutics
ISSN: 1744-8360
Titre abrégé: Expert Rev Neurother
Pays: England
ID NLM: 101129944
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
pubmed:
23
4
2020
medline:
18
5
2021
entrez:
23
4
2020
Statut:
ppublish
Résumé
Infantile spasm (IS) is an epileptic syndrome with typical onset within the first 2 years of life. This condition might be caused by several etiologies. IS is associated with pathological neuronal networks; however, definite hypotheses on neurobiological processes are awaited. Changes in NMDA and GABA Recently, no new therapeutic options for IS have emerged, probably due to the lack of reliable animal models and to the extreme variability in etiologies. Consequently, the outlook for patients and families is poor and early recognition and intervention remain research priorities.
Identifiants
pubmed: 32316776
doi: 10.1080/14737175.2020.1759423
doi:
Substances chimiques
Anticonvulsants
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM