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Objective: Semiology-based preoperative anatomical hypotheses are necessary, yet comprehensive reports on the semiology and its correlation with central subregions in central epilepsy has still lacked. We wished to identify semiologic subgroups and their correlations with central subregions.
Methods: We retrospectively included 21 patients with central epilepsy identified by stereoelectroencephalography (sEEG). The central region was segmented into 12 subregions using the Human Brainnetome Atlas, and both sEEG data and semiology underwent quantitative analysis.
Results: We defined three patient groups based on semiologic pattern similarities. Several intriguing anatomical-electroclinical correlations were initially observed, including the involvement of paracentral lobule (PCL) subregion 2 in upper-limb sensations, PCL1 in autonomic signs, and notably, postcentral gyrus (PoG) 2 in orofacial motor signs and precentral gyrus (PrG) 1 in hand sensations, which may be explained by the overlap among motor and sensory cortices, suggesting a reexamination of traditional localizations of somatosensory or motor signs to the PoG or PrG. Furthermore, anatomic structures initiating ictal signs constructed specific early spread networks. While all patient groups exhibited propagation to the parietal (P) and cingulate cortices (CG), ictal discharges originating from the superior, the posterior-inferior (near the lateral sulcus), and the middle-inferior aspects tended to propagate anteriorly toward the frontal lobe, in a superior direction and to the adjacent insula, and in a bidirectional manner-that is, towards the middle-front and the posterior regions, respectively.
Conclusion: Localizing semiology to central subregions and mapping clinical patterns to early spread networks allowed central epilepsy dynamics to be realized and helped define the range of epileptogenic anomalies preoperatively.
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http://dx.doi.org/10.1016/j.yebeh.2025.110662 | DOI Listing |
Am J Hum Genet
September 2025
Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, Rotterdam 3000 CA, the Netherlands.
Microtubule-actin cross-linking factor 1 (MACF1) is a large protein of the spectraplakin family, which is essential for brain development. MACF1 interacts with microtubules through the growth arrest-specific 2 (Gas2)-related (GAR) domain. Heterozygous MACF1 missense variants affecting the zinc-binding residues in this domain result in a distinctive cortical and brain stem malformation.
View Article and Find Full Text PDFChilds Nerv Syst
September 2025
Department of Pediatrics, NAMO Medical Education and Research Institute, Silvassa, Dadra and Nagar Haveli, India.
Introduction: Neurocysticercosis (NCC) is a parasitic infection of the central nervous system caused by the ingestion of Taenia solium eggs, typically through the consumption of undercooked pork or contaminated water. Recognized as a leading preventable cause of epilepsy, NCC poses a significant public health challenge, particularly in developing nations such as India. This retrospective observational study aimed to investigate the clinical manifestations, radiological characteristics, diagnostic approaches, therapeutic interventions, and follow-up outcomes of pediatric patients diagnosed with NCC.
View Article and Find Full Text PDFFASEB J
September 2025
Department of Hematology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, People's Republic of China.
Epilepsy is a common chronic nervous system disease that threatens human health. However, the role of FOXC1 and its relations with pyroptosis have not been fully studied in epilepsy. Sprague-Dawley rats were obtained for constructing temporal lobe epilepsy (TLE) models.
View Article and Find Full Text PDFJ Integr Neurosci
August 2025
Central Laboratory, The First Affiliated Hospital of Henan Polytechnic University (Jiaozuo Second People's Hospital), 454001 Jiaozuo, Henan, China.
Background: Epilepsy, a significant neurological condition marked by the occurrence of repeated seizures, continues to pose a substantial health challenge. Previous studies have indicated that Dipeptidyl Peptidase-4 (DPP4) inhibitors may possess antiepileptic properties. Ferroptosis, a newly discovered type of programmed cell death, has recently surfaced as a promising therapeutic target in the management of epilepsy.
View Article and Find Full Text PDFImmune Netw
August 2025
Department of Microbiology and Immunology, Yonsei University College of Medicine, Seoul 03722, Korea.
Developmental and epileptic encephalopathies (DEEs), including Infantile Epileptic Spasms Syndrome (IESS) and Lennox-Gastaut Syndrome (LGS), are severe pediatric conditions characterized by profound developmental delays and treatment-resistant epilepsy. Although steroid therapies provide some clinical benefits, the underlying immunological mechanisms remain poorly understood. In this study, we performed comprehensive immune profiling using multi-parametric flow cytometry on PBMCs from IESS (n=25) and LGS (n=9) patients, comparing them with age-matched healthy controls (n=54).
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