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Myoclonic epilepsy refers to a family of epilepsies that present with myoclonus. When myoclonic jerks are occasionally associated with abnormal brain wave activity, it can be categorized as myoclonic seizure.
8 Μαΐ 2023 · Myoclonic epilepsy of infancy (MEI) is a rare self-limited epileptic syndrome characterized by brief myoclonic seizures in previously healthy and developmentally normal children with onset in the first three years of life.
The world’s foremost experts describe the phenotypes and subtypes of myoclonic epilepsies and the underlying molecular defects and summarize cutting-edge advances in molecular genetics that...
Progressive Myoclonic Epilepsies (PME) are a rare group of inherited neurodegenerative diseases characterized by myoclonus, resistance to treatment, and neurological deterioration. [2] The cause of PME depends largely on the type of PME.
Progressive Myoclonus Epilepsies (PMEs) are a group of uncommon clinically and genetically heterogeneous disorders characterised by myoclonus, generalized epilepsy, and neurological deterioration, including dementia and ataxia.
24 Ιουν 2004 · Progressive myoclonic epilepsy type 1 (EPM1) is a neurodegenerative disorder characterized by onset from age six to 15 years, stimulus-sensitive myoclonus, and tonic-clonic epileptic seizures. Some years after the onset, ataxia, incoordination, intentional tremor, and dysarthria develop.
8 Μαΐ 2023 · Myoclonic epilepsy of infancy (MEI) is a rare self-limited epileptic syndrome characterized by brief myoclonic seizures in previously healthy and developmentally normal children with onset in the first three years of life.
