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content:epileptic_encephalopathies [2020/02/16 22:28] – icna | content:epileptic_encephalopathies [2020/02/16 22:29] – [Epileptic encephalopathies] icna | ||
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Epileptic encephalopathies are a heterogenous group of conditions where the epileptic activity itself contributes to severe cognitive and behavioral impairments above and beyond what might be expected from the underlying pathology alone (e.g., cortical malformation), | Epileptic encephalopathies are a heterogenous group of conditions where the epileptic activity itself contributes to severe cognitive and behavioral impairments above and beyond what might be expected from the underlying pathology alone (e.g., cortical malformation), | ||
- | The recognized epileptic encephalopathies currently are [[Early Myoclonic Encephalopathy]], [[Early Infantile Epileptic Encephalopathy]] ([[Ohtahara Syndrome]]), [[Epilepsy of infancy with migrating focal seizures]], [[West Syndrome]], [[Dravet Syndrome]], [[Epilepsy with Myoclonic Astatic Seizures]], [[Lennox-Gastaut Syndrome]], and [[Epilepsy with Continuous Spike-Waves during Slow Wave Sleep]] including [[Landau-Kleffner Syndrome]] and [[Atypical Benign Partial Epilepsy]]. | + | The recognized epileptic encephalopathies currently are |
+ | * [[Early Myoclonic Encephalopathy]] | ||
+ | * [[Early Infantile Epileptic Encephalopathy]] ([[Ohtahara Syndrome]]) | ||
+ | * [[Epilepsy of infancy with migrating focal seizures]] | ||
+ | * [[West Syndrome]], [[Dravet Syndrome]] | ||
+ | * [[Epilepsy with Myoclonic Astatic Seizures]] | ||
+ | * [[Lennox-Gastaut Syndrome]] | ||
+ | * [[Epilepsy with Continuous Spike-Waves during Slow Wave Sleep]] including [[Landau-Kleffner Syndrome]] and [[Atypical Benign Partial Epilepsy]]. | ||
One approach to epileptic encephalopathies is based on whether the presentation is with seizures as a prominent/ | One approach to epileptic encephalopathies is based on whether the presentation is with seizures as a prominent/ |