MECP2 duplication syndrome: The electroclinical features of a case with long-term evolution

MECP2 duplication syndrome (MDS) is a rare and severe neurodevelopmental disorder frequently associated with epilepsy. Different seizure types and electroencephalographic (EEG) patterns were described in patients with MDS, although it lacks a specific phenotype. We report on an adult patient with lo...

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Detalles Bibliográficos
Autores principales: Cani, Ilaria, Muccioli, Lorenzo, Mignani, Francesco, Licchetta, Laura, Tinuper, Paolo, Provini, Federica, Bisulli, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062211/
https://www.ncbi.nlm.nih.gov/pubmed/35520952
http://dx.doi.org/10.1016/j.ebr.2022.100541

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062211/
https://www.ncbi.nlm.nih.gov/pubmed/35520952
http://dx.doi.org/10.1016/j.ebr.2022.100541

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