Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome

Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome

Abstract Background Rett syndrome is a neurodevelopmental disorder caused by a mutation in the X-linked MECP2 gene. Individuals with Rett syndrome typically develop normally until around 18 months of age before undergoing a developmental regression, and the disorder can lead to cognitive, motor, sen...

Full description

Bibliographic Details
Main Authors: Katherine J. Roche, Jocelyn J. LeBlanc, April R. Levin, Heather M. O’Leary, Lauren M. Baczewski, Charles A. Nelson
Format: Article
Language:English
Published: BMC 2019-07-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Rett syndrome
EEG
Electroencephalography
Spectral power
Electrophysiology
Biomarker
Online Access:http://link.springer.com/article/10.1186/s11689-019-9275-z

Internet

http://link.springer.com/article/10.1186/s11689-019-9275-z

Similar Items