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Case report: Dravet syndrome, feeding difficulties and gastrostomy

Dravet syndrome (DS) is a developmental and epileptic encephalopathy associated with variants in the voltage-gated sodium channel alpha 1 subunit (SCN1A) gene in around 90% of individuals. The core phenotype is well-recognized, and is characterized by seizure onset in infancy, typically with prolong...

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Detalles Bibliográficos
Autores principales: Clayton, Lisa M., Williams, Edwina, Balestrini, Simona, Sisodiya, Sanjay M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513453/
https://www.ncbi.nlm.nih.gov/pubmed/36176564
http://dx.doi.org/10.3389/fneur.2022.993906

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