Early infantile epileptic encephalopathy type 16: the new clinical and genetic variant of TBC1D24 gene mutation
Objective: to analyse the clinical and neurophysiological data from a case of early infantile epileptic encephalopathy type 16 in a child with homozygous mutation in TBC1D24 gene.Material and methods. Female child M. aged 1 year and 2 months, with identified mutations in TBC1D24 gene was examined. T...
Main Authors: | A. A. Kholin, I. D. Fedonyuk, O. P. Dovelman, N. N. Zavadenko, T. V. Kozhanova, E. A. Kholina, G. Sh. Khondkarian, E. S. Il`ina |
---|---|
Format: | Article |
Language: | Russian |
Published: |
IRBIS LLC
2020-01-01
|
Series: | Эпилепсия и пароксизмальные состояния |
Subjects: | |
Online Access: | https://www.epilepsia.su/jour/article/view/499 |
Similar Items
-
Early infantile epileptic encephalopathy type 4: clinical, neurophysiological and therapeutic aspects
by: A. A. Kholin, et al.
Published: (2019-07-01) -
A dramatic EEG response to fenfluramine in a patient with developmental and epileptic encephalopathy
by: Douglas R. Nordli III, et al.
Published: (2024-03-01) -
EFFICACY AND SAFETY OF LEVETIRACETAM IN CHILDREN WITH ELECTRICAL STATUS EPILEPTICUS DURING SLOW-WAVE SLEEP (ESES)
by: A. A. Kholin, et al.
Published: (2017-08-01) -
Ictal and interictal electroencephalographic findings can contribute to early diagnosis and prompt treatment in KCNQ2-associated epileptic encephalopathy
by: Inn-Chi Lee, et al.
Published: (2021-01-01) -
Epileptic Encephalopathies, CDKL5 Mutations, and Infantile Spasms
by: J Gordon Millichap
Published: (2012-02-01)