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SYNGAP1-DEE: A visual sensitive epilepsy.
Lo Barco, Tommaso; Kaminska, Anna; Solazzi, Roberta; Cancés, Claude; Barcia, Giulia; Chemaly, Nicole; Fontana, Elena; Desguerre, Isabelle; Canafoglia, Laura; Hachon Le Camus, Caroline; Losito, Emma; Villard, Laurent; Eisermann, Monika; Dalla Bernardina, Bernardo; Villeneuve, Nathalie; Nabbout, Rima.
Afiliación
  • Lo Barco T; Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France; Child Neuropsychiatry, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy; PhD Progr
  • Kaminska A; Department of Clinical Neurophysiology, Necker-Enfants-Malades Hospital, AP-HP, Paris, France.
  • Solazzi R; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
  • Cancés C; Department of Pediatric Neurology, Toulouse Children Hospital, Toulouse University Hospital, Toulouse, France.
  • Barcia G; Fédération de Génétique Médicale, Hôpital Necker-Enfants Malades, Paris, France.
  • Chemaly N; Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France; Department of Paediatric Neurology, Necker-Enfants Malades Hospital, University of Paris, AP-HP, Paris, France.
  • Fontana E; Child Neuropsychiatry, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy; Research Center for Pediatric Epilepsies Verona, Verona, Italy.
  • Desguerre I; Department of Paediatric Neurology, Necker-Enfants Malades Hospital, University of Paris, AP-HP, Paris, France.
  • Canafoglia L; Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
  • Hachon Le Camus C; Department of Pediatric Neurology, Toulouse Children Hospital, Toulouse University Hospital, Toulouse, France.
  • Losito E; Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France.
  • Villard L; Pediatric Neurology Department, Timone Children Hospital, Reference Center for Rare Epilepsies, APHM, Marseille, France.
  • Eisermann M; Department of Clinical Neurophysiology, Necker-Enfants-Malades Hospital, AP-HP, Paris, France.
  • Dalla Bernardina B; Research Center for Pediatric Epilepsies Verona, Verona, Italy.
  • Villeneuve N; Pediatric Neurology Department, Timone Children Hospital, Reference Center for Rare Epilepsies, APHM, Marseille, France.
  • Nabbout R; Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France; Department of Paediatric Neurology, Necker-Enfants Malades Hospital, University of Paris, AP-HP, Paris, France. Electronic address:
Clin Neurophysiol ; 132(4): 841-850, 2021 04.
Article en En | MEDLINE | ID: mdl-33639450
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Epilepsias Mioclónicas / Epilepsia Refleja / Proteínas Activadoras de ras GTPasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Neurophysiol Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Epilepsias Mioclónicas / Epilepsia Refleja / Proteínas Activadoras de ras GTPasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Neurophysiol Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA Año: 2021 Tipo del documento: Article