PRRT2‐positive self‐limited infantile epilepsy: Initial seizure characteristics and response to sodium channel blockers
Abstract Objective Self‐limited infantile epilepsy (SeLIE) has distinctive clinical features, and the PRRT2 gene is known to be a considerable genetic cause. There have been a few studies on PRRT2‐positive SeLIE only, and anti‐seizure medications are often required due to frequent seizures at initia...
Main Authors: | Jiwon Lee, Young Ok Kim, Byung Chan Lim, Jeehun Lee |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2023-06-01
|
Series: | Epilepsia Open |
Subjects: | |
Online Access: | https://doi.org/10.1002/epi4.12708 |
Similar Items
-
Epilepsy Spectrum Associated with PRRT2 Variants: Case Presentations
by: Semı̇h Taşdelen, et al.
Published: (2023-12-01) -
Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant
by: Yu Gu, et al.
Published: (2023-05-01) -
Levetiracetam may be an unsuitable choice for patients with PRRT2-associated self-limited infantile epilepsy
by: Yang Tian, et al.
Published: (2023-10-01) -
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood
by: Jan Henje Döring, et al.
Published: (2020-10-01) -
CONCOMITANCE OF INFANTILE AUTISM AND EPILEPSY: ETIOPATHOGENIC ASPECTS
by: E. V. Malinina, et al.
Published: (2009-03-01)