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Article

Reviewing Evidence for the Relationship of EEG Abnormalities and RTT Phenotype Paralleled by Insights from Animal Studies.

International journal of molecular sciences - 18 May 2021

Smirnov Kirill, Stroganova Tatiana, Molholm Sophie, Sysoeva Olga

Abstract excerpt

Rett syndrome (RTT) is a rare neurodevelopmental disorder that is usually caused by mutations of the MECP2 gene. Patients with RTT suffer from severe deficits in motor, perceptual and cognitive domains. Electroencephalogram (EEG) has provided useful information to clinicians and scientists, from the very first descriptions of RTT, and yet no reliable neurophysiological biomarkers related to the pathophysiology of...

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Identifiers

PMID: 34069993
DOI: 10.3390/ijms22105308
PMCID: PMC8157853

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