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Expanding the Treatment Landscape for Lennox-Gastaut Syndrome: Current and Future Strategies

Lennox-Gastaut syndrome (LGS), a childhood-onset severe developmental and epileptic encephalopathy (DEE), is an entity that encompasses a heterogenous group of aetiologies, with no single genetic cause. It is characterised by multiple seizure types, an abnormal EEG with generalised slow spike and wa...

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Detalles Bibliográficos
Autores principales: Strzelczyk, Adam, Schubert-Bast, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873005/
https://www.ncbi.nlm.nih.gov/pubmed/33479851
http://dx.doi.org/10.1007/s40263-020-00784-8