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Ictal asystole is a rare condition associated primarily with temporal lobe epilepsy that can cause syncope, falls, and head trauma. It is also associated with increased rates of sudden unexplained death in epilepsy. We present a case of a 33-year-old woman with a history of childhood epilepsy who presented with 3 years of recurrent syncope. Video-EEG revealed temporal lobe seizures with ictal asystole. EKG showed stepwise progression of bradycardia, asystole, and tachycardia. MRI showed focal cortical thickening at the right insular cortex with blurring of the gray-white matter interface, consistent with insular focal cortical dysplasia. The patient was transitioned from lacosamide to clobazam because of concern for PR interval prolongation and was referred to cardiology for pacemaker placement. Ictal asystole should be considered as a rare but serious cause of unexplained recurrent syncope, particularly in patients with a history of seizures. Management includes antiepileptic drug regimen optimization, consideration of epilepsy surgery, and referral for cardiac pacing when asystole lasts longer than 6 seconds.
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http://dx.doi.org/10.1212/WNL.0000000000207396 | DOI Listing |
Clin Genet
October 2025
Department of Neuropediatrics, CréER, ERN EpiCare, Strasbourg University Hospitals, Strasbourg, France.
We report the first known case of a 9-year-old male with early-onset epilepsy, syncope, and ictal asystole-requiring pacemaker implantation at the age of seven-associated with a pathogenic variant in FGF12.
View Article and Find Full Text PDFJ ECT
August 2025
Noninvasive Neurostimulation Therapies Laboratory, Department of Psychiatry.
Ann Neurol
August 2025
Computational Neurology, Department of Neurology and Berlin Institute of Health, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Objective: Prognostication in patients with disorders of consciousness (DOCs) remains challenging because of heterogeneous etiologies, pathophysiologies and, consequently, highly variable electroencephalograms (EEGs). Here, we use EEG patterns that are well-characterizable to create a latent map that positions novel EEGs along a continuum. We asses this map as a generalizable tool to extract prognostically valuable information from long-term EEG, by predicting outcome post-cardiac arrest as a first use case.
View Article and Find Full Text PDFEpileptic Disord
August 2025
Department of Neurosurgery, Nara Medical University, Nara, Japan.
Content available: Video
View Article and Find Full Text PDFJ Transl Med
April 2025
Department of Pharmacology, SUNY Upstate Medical University, Syracuse, NY, USA.
Background: Long QT Syndrome Type-2 (LQT2) is due to loss-of-function KCNH2 variants. KCNH2 encodes K11.1 that forms a delayed-rectifier potassium channel in the brain and heart.
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