The purpose of this study was to assess the cortical representation of sensorimotor functions in patients undergoing perirolandic epilepsy surgery, focusing on somatotopy, mosaicism, and variability of function in relation to the classic motor homunculus. The authors studied 36 patients in whom intraoperative or extraoperative electrical cortical stimulation to map motor functions was performed. A computer program was devised to register electrode number, stimulation parameters, and response to each stimulus. Electrode position was represented graphically whenever a stimulus was delivered. A total of 43 maps from 36 patients were analyzed. The authors found variations in the organization of M1 (primary motor cortex) in seven patients (19.4%). Four patients (11.1%) presented mosaicism (overlapping of functional areas), two (5.6%) presented variability (inverted disposition of M1 functional areas), and one (2.8%) had both. The results of this study challenge the notion of orderly topographic relationships between the human sensorimotor functions and their representation in the primary motor cortex. These results confirm those of other studies with animals and humans using novel imaging techniques, suggesting that the motor homunculus may not always be considered a definite and absolute representation of M1.
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http://dx.doi.org/10.1097/00004691-200302000-00002 | DOI Listing |
J Neurosurg Case Lessons
October 2024
Brain and Development Research Axis, Sainte-Justine University Hospital Research Center, Montréal, Québec, Canada.
J Clin Neurophysiol
October 2024
Division of Neurology, Comprehensive Epilepsy Center, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, U.S.A.
Epilepsia
November 2024
Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Am J Med Genet A
January 2025
Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
We studied three brothers and a maternal half-brother featuring global developmental delay, mild to moderate intellectual disability, epilepsy, microcephaly, and strabismus. All had bilateral perisylvian and perirolandic polymicrogyria, while some also had malformations of the hippocampus (malrotation and dysplasia), cerebellum (heterotopias and asymmetric aplasia), corpus callosum dysgenesis, and brainstem asymmetric dysplasia. Exome sequencing showed that all four patients had a novel variant (c.
View Article and Find Full Text PDFNeurol Clin Pract
April 2024
Epilepsy Center (NF, AA, KP, AM, MV, GF-B, HL), Neurological Institute, University Hospitals Cleveland Medical Center, OH; Department of Neurology (NF, GF-B, HL), Case Western Reserve University School of Medicine; and Epilepsy Center (SH), University of Melbourne, Australia.
Background And Objectives: Clonic seizures are currently defined as repetitive and rhythmic contractions of a specific body part, producing twitching movements at a frequency of 0.2-5 Hz. There are few studies in the literature that have reported a detailed analysis of the semiology, neurophysiology, and lateralizing value of clonic seizures.
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