Cargando…
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...
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 |
Ejemplares similares
-
Audit of use of stiripentol in adults with Dravet syndrome
por: Balestrini, S., et al.
Publicado: (2016) -
The impact of COVID‐19 in Dravet syndrome: A UK survey
por: Balestrini, Simona, et al.
Publicado: (2021) -
The impact of SARS-CoV-2 vaccination in Dravet syndrome: A UK survey
por: Clayton, Lisa M., et al.
Publicado: (2021) -
Late diagnoses of Dravet syndrome: How many individuals are we missing?
por: Silvennoinen, Katri, et al.
Publicado: (2021) -
Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes
por: Ding, Jiangwei, et al.
Publicado: (2022)