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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...
Autores principales: | Moschopoulos, Chariton, Peters, Jurriaan M., Takeoka, Masanori, Stredny, Coral M. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
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 |
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