Continuous spike-and-wave activity during slow-wave sleep in patients with rett syndrome

The article presents a description of a clinical case of a child 3 years 8 months old with Rett syndrome caused by the mutation of p.Val485fs in the MECP2 gene. According to electroencephalography data at the age of 1 year and 6 months, diffuse continued epileptiform activity in the form of high-amp...

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Bibliographic Details
Main Authors: S. L. Kulikova, I. V. Kozyreva, S. A. Likhachev, M. Yu. Bobylova
Format: Article
Language:Russian
Published: ABV-press 2021-07-01
Series:Русский журнал детской неврологии
Subjects:
Online Access:https://rjdn.abvpress.ru/jour/article/view/363