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20 de may. de 2024 · Lennox-Gastaut syndrome (LGS) is a severe form of epilepsy that typically becomes apparent during infancy or early childhood. Affected children experience several different types of seizures, most commonly atonic, tonic and atypical absence seizures.
10 de may. de 2024 · The Refractory Epilepsy Screening Tool for Lennox Gastaut syndrome (REST-LGS) can be used to screen patients with drug-resistant epilepsy in the clinical setting. Of the 100 patients in this retrospective analysis, the majority (56–71%) met 4 of 8 REST-LGS criteria, and all 4 major REST-LGS criteria were met in 22 patients (22%).
10 de may. de 2024 · Objective: To evaluate the Refractory Epilepsy Screening Tool for Lennox-Gastaut Syndrome (REST-LGS) for real-world identification of LGS in adults and to develop a scoring system for the tool. Methods: A retrospective chart review of adults with drug resistant epilepsy (DRE) and intellectual development disorder (IDD) was conducted ...
14 de may. de 2024 · Lennox-Gastaut syndrome (LGS), a type of DEE, is characterized by an electroclinical trend of generalized slow spike wave activity in the EEG, multiple types of epileptic seizures, and slow mental development.
22 de may. de 2024 · The Refractory Epilepsy Screening Tool for Lennox–Gastaut Syndrome (REST-LGS) can identify most patients who were previously undiagnosed as “possibly” or “likely” having LGS, according to a new study published in the journal Epilepsia Open.
7 de may. de 2024 · This paper outlines the therapeutic rationale and neurosurgical targeting technique for bilateral, closed-loop, thalamocortical stimulation in Lennox-Gastaut syndrome, a severe form of childhood-onset epilepsy.
20 de may. de 2024 · The goal of this activity is to educate all neurologists to become familiar with Lennox-Gastaut syndrome (LGS) and recognize the changes in symptoms as well as personal and social needs in patients as they progress from childhood to adolescence and adulthood.
