Candidate Genes for Eyelid Myoclonia with Absences, Review of the Literature

Candidate Genes for Eyelid Myoclonia with Absences, Review of the Literature

Eyelid myoclonia with absences (EMA), also known as Jeavons syndrome (JS) is a childhood onset epileptic syndrome with manifestations involving a clinical triad of absence seizures with eyelid myoclonia (EM), photosensitivity (PS), and seizures or electroencephalogram (EEG) paroxysms induced by eye...

Full description

Bibliographic Details
Main Authors: Sonia Mayo, Irene Gómez-Manjón, Fco. Javier Fernández-Martínez, Ana Camacho, Francisco Martínez, Julián Benito-León
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:International Journal of Molecular Sciences
Subjects:
Jeavons syndrome
eyelid myoclonia with absences
candidate genes
<i>SYNGAP1</i>
<i>KIA02022</i>
<i>NEXMIF</i>
Online Access:https://www.mdpi.com/1422-0067/22/11/5609

Similar Items

Similar Items