SYNGAP1-DEE: A visual sensitive epilepsy

Clin Neurophysiol. 2021 Apr;132(4):841-850. doi: 10.1016/j.clinph.2021.01.014. Epub 2021 Feb 3.

Abstract

Objective: To further delineate the electroclinical features of individuals with SYNGAP1 pathogenic variants.

Methods: Participants with pathogenic SYNGAP1 variants and available video-electroencephalogram (EEG) recordings were recruited within five European epilepsy reference centers. We obtained molecular and clinical data, analyzed EEG recordings and archived video-EEGs of seizures and detailed characteristics of interictal and ictal EEG patterns for every patient.

Results: We recruited 15 previously unreported patients and analyzed 72 EEGs. Two distinct EEG patterns emerged, both triggered by eye closure. Pattern 1 (14/15 individuals) consisted of rhythmic posterior/diffuse delta waves appearing with eye-closure and persisting until eye opening (strongly suggestive of fixation-off sensitivity). Pattern 2 (9/15 individuals) consisted of diffuse polyspike-and-wave discharges triggered by eye closure (eye-closure sensitivity). Both patterns presented in 8/15. Including archived video-EEG clips of seizures from 9/15 patients, we analyzed 254 seizures. Of 224 seizures experienced while awake, 161 (72%) occurred at or following eye closure. In 119/161, pattern 1 preceded an atypical absence, myoclonic seizure or myoclonic absence; in 42/161, pattern 2 was associated with eyelid myoclonia, absences and myoclonic or atonic seizures.

Conclusions: Fixation-off and eye closure were the main triggers for seizures in this SYNGAP1 cohort.

Significance: Combining these clinical and electroencephalographic features could help guide genetic diagnosis.

Keywords: Eye-closure sensitivity; Fixation-off sensitivity; Myoclonic seizures; Photosensitivity; Reflex epilepsy; SYNGAP1.

MeSH terms

  • Adolescent
  • Brain / physiopathology*
  • Child
  • Child, Preschool
  • Electroencephalography
  • Epilepsies, Myoclonic / diagnosis*
  • Epilepsies, Myoclonic / genetics
  • Epilepsies, Myoclonic / physiopathology
  • Epilepsy, Reflex / diagnosis*
  • Epilepsy, Reflex / genetics
  • Epilepsy, Reflex / physiopathology
  • Female
  • Humans
  • Infant
  • Male
  • ras GTPase-Activating Proteins / genetics*

Substances

  • SYNGAP1 protein, human
  • ras GTPase-Activating Proteins