Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/86619
Title: Clinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizures
Authors: Crunelli, Vincenzo
Lőrincz, Magor L.
McCafferty, Cian P.
Lambert, Régis C.
Leresche, Nathalie
Di Giovanni, Giuseppe
David, Francois
Keywords: Petit mal epilepsy -- Treatment
Petit mal epilepsy -- Drug therapy
Petit mal epilepsy -- Animal models
Petit mal epilepsy -- Alternative treatment
Basal ganglia -- Pathophysiology
Limbic system
Issue Date: 2020
Publisher: Oxford University Press
Citation: Crunelli, V., Lőrincz, M. L., McCafferty, C., Lambert, R. C., Leresche, N., Di Giovanni, G., & David, F. (2020). Clinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizures. Brain, 143(8), 2341-2368.
Abstract: Absence seizures in children and teenagers are generally considered relatively benign because of their non-convulsive nature and the large incidence of remittance in early adulthood. Recent studies, however, show that 30% of children with absence seizures are pharmaco-resistant and 60% are affected by severe neuropsychiatric comorbid conditions, including impairments in attention, cognition, memory and mood. In particular, attention deficits can be detected before the epilepsy diagnosis, may persist even when seizures are pharmacologically controlled and are aggravated by valproic acid monotherapy. New functional MRI-magnetoencephalography and functional MRI-EEG studies provide conclusive evidence that changes in blood oxygenation level-dependent signal amplitude and frequency in children with absence seizures can be detected in specific cortical networks at least 1 min before the start of a seizure, spike-wave discharges are not generalized at seizure onset and abnormal cortical network states remain during interictal periods. From a neurobiological perspective, recent electrical recordings and imaging of large neuronal ensembles with single-cell resolution in non-anaesthetized models show that, in contrast to the predominant opinion, cortical mechanisms, rather than an exclusively thalamic rhythmogenesis, are key in driving seizure ictogenesis and determining spike-wave frequency. [Excerpt from Abstract]
URI: https://www.um.edu.mt/library/oar/handle/123456789/86619
Appears in Collections:Scholarly Works - FacM&SPB



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