An Overview of the Electroencephalographic (EEG) Features of Epilepsy with Eyelid Myoclonia (Jeavons Syndrome).
Eyelid myoclonia
Jeavons Syndrome
genetic generalized epilepsy
Journal
The Neurodiagnostic journal
ISSN: 2164-6821
Titre abrégé: Neurodiagn J
Pays: United States
ID NLM: 101573167
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
pubmed:
6
5
2020
medline:
7
4
2021
entrez:
6
5
2020
Statut:
ppublish
Résumé
Epilepsy with eyelid myoclonia or Jeavons Syndrome is a unique idiopathic generalized epilepsy with onset in childhood. It is characterized by eyelid myoclonia which may be associated with absence seizures, eyelid closure-induced epileptiform discharges and/or seizures and photosensitivity. It is frequently underrecognized and misdiagnosed because it may be mistaken for some other type of generalized epilepsy or facial tic disorder. The intent of this narrative review is to focus on existing literature and highlight the distinct electroencephalographic features including characteristic eye movements, associated waveforms, interictal and ictal findings that are suggestive and characteristic of Jeavons Syndrome to aid in timely recognition of this syndrome.
Identifiants
pubmed: 32369428
doi: 10.1080/21646821.2020.1750879
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM