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...
Main Authors: | , , , |
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Format: | Article |
Language: | Russian |
Published: |
ABV-press
2021-07-01
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Series: | Русский журнал детской неврологии |
Subjects: | |
Online Access: | https://rjdn.abvpress.ru/jour/article/view/363 |