Infantile Hemiconvulsion-Hemiplegia and Epilepsy (IHHE) in a boy with tuberous sclerosis complex

Tuberous sclerosis complex (TSC) is a rare autosomal dominant disease due to pathogenic variants in TSC1 or TSC2 genes. In the brain, TSC is associated with multiple cortical and subcortical malformations including tubers and abnormalities of radial neuronal migration. Approximately 80% of patients...

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Detalles Bibliográficos
Autores principales: Moschopoulos, Chariton, Peters, Jurriaan M., Takeoka, Masanori, Stredny, Coral M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383053/
https://www.ncbi.nlm.nih.gov/pubmed/34466799
http://dx.doi.org/10.1016/j.ebr.2021.100473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383053/
https://www.ncbi.nlm.nih.gov/pubmed/34466799
http://dx.doi.org/10.1016/j.ebr.2021.100473

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