The feasibility of using actigraphy to characterize sleep in Rett syndrome

Abstract Background Rett syndrome (RTT) is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene. Sleep problems are reported by the majority of caregivers of individuals with RTT. Methods The present study aimed to replicate and extend previous work about the feasibility of...

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Bibliographic Details
Main Authors: Alyssa M. Merbler, Breanne J. Byiers, John J. Garcia, Timothy J. Feyma, Frank J. Symons
Format: Article
Language:English
Published: BMC 2018-02-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s11689-018-9227-z