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content:epileptic_encephalopathies [2020/02/16 22:29] – [Epileptic encephalopathies] icna | content:epileptic_encephalopathies [2022/04/30 11:54] (current) – changed pubmed syntax administrator@icnapedia.org | ||
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====== Epileptic encephalopathies ====== | ====== Epileptic encephalopathies ====== | ||
- | 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 | + | The report of the International League Against Epilepsy (ILAE) Task Force on classification and terminology includes 8 syndromes under epileptic encephalopathies: |
* [[Early Myoclonic Encephalopathy]] | * [[Early Myoclonic Encephalopathy]] | ||
* [[Early Infantile Epileptic Encephalopathy]] ([[Ohtahara Syndrome]]) | * [[Early Infantile Epileptic Encephalopathy]] ([[Ohtahara Syndrome]]) | ||
* [[Epilepsy of infancy with migrating focal seizures]] | * [[Epilepsy of infancy with migrating focal seizures]] | ||
- | * [[West Syndrome]], [[Dravet Syndrome]] | + | * [[West Syndrome]] |
+ | * [[Dravet Syndrome]] | ||
* [[Epilepsy with Myoclonic Astatic Seizures]] | * [[Epilepsy with Myoclonic Astatic Seizures]] | ||
* [[Lennox-Gastaut Syndrome]] | * [[Lennox-Gastaut Syndrome]] | ||
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==== Presenting with seizures associated with a syndromic phenotype ==== | ==== Presenting with seizures associated with a syndromic phenotype ==== | ||
- | * **Chromosomopathies** | + | * **Chromosomal abnormalities** |
* [[1p36 monosomy]] | * [[1p36 monosomy]] | ||
* [[Wolf-Hirschhorn syndrome]] | * [[Wolf-Hirschhorn syndrome]] |