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...

Full description

Bibliographic Details
Main Authors: Galina Portnova, Anastasia Neklyudova, Victoria Voinova, Olga Sysoeva
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Journal of Personalized Medicine
Subjects:
Online Access:https://www.mdpi.com/2075-4426/12/12/1973