Secular changes in severity of intellectual disability in tuberous sclerosis complex: A reflection of improved identification and treatment of epileptic spasms?

Tuberous sclerosis complex (TSC) is a multisystem genetic disorder caused by mutations in TSC1 or TSC2. Epilepsy occurs in 80%‐90% of affected individuals during their lifetime, and up to one‐third of children with TSC will develop epileptic (infantile) spasms, for which vigabatrin has been shown to...

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Detalhes bibliográficos
Publicado no:Epilepsia Open
Main Authors: Tye, Charlotte, Thomas, Laura E., Sampson, Julian R., Lewis, Julia, O'Callaghan, Finbar, Yates, John R. W., Bolton, Patrick F.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Short Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5983114/
https://ncbi.nlm.nih.gov/pubmed/29881807
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/epi4.12111
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