Clinical EEG of Rett Syndrome: Group Analysis Supplemented with Longitudinal Case Report

Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is characterized by atypical EEG activity, and its detailed examination is lacking. We combined the comparison of one-time eyes open EEG resting state activity from 32 girls with RTT and their 41 typically...

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Detalles Bibliográficos
Autores principales: Portnova, Galina, Neklyudova, Anastasia, Voinova, Victoria, Sysoeva, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782488/
https://www.ncbi.nlm.nih.gov/pubmed/36556193
http://dx.doi.org/10.3390/jpm12121973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782488/
https://www.ncbi.nlm.nih.gov/pubmed/36556193
http://dx.doi.org/10.3390/jpm12121973

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