pubmed-article:17961983 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0497327 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0014544 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0013080 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0014550 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0868928 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0332162 | lld:lifeskim |
pubmed-article:17961983 | lifeskim:mentions | umls-concept:C0205087 | lld:lifeskim |
pubmed-article:17961983 | pubmed:issue | 2-3 | lld:pubmed |
pubmed-article:17961983 | pubmed:dateCreated | 2007-11-26 | lld:pubmed |
pubmed-article:17961983 | pubmed:abstractText | Senile myoclonic epilepsy of Genton is a newer epileptic syndrome of the older patients with Down syndrome associated with an Alzheimer-type dementia. We report two observations in whom the clinical and electroencephalographic features are consistent with the description of this syndrome. Both experienced a progressive deterioration of cognitive functions few years before the onset of the epilepsy. The EEG was characteristic with generalized fast spike-waves or polyspikes or polyspike-waves with or without bilateral myoclonic jerks especially at awakenings. One patient had a photoparoxysmal response (11-21Hz) with bilateral myoclonic jerks. Hence, the senile myoclonic epilepsy of Genton is an easily recognizable newer epileptic syndrome of the older Down syndrome patient. | lld:pubmed |
pubmed-article:17961983 | pubmed:language | eng | lld:pubmed |
pubmed-article:17961983 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17961983 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17961983 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17961983 | pubmed:month | Dec | lld:pubmed |
pubmed-article:17961983 | pubmed:issn | 0920-1211 | lld:pubmed |
pubmed-article:17961983 | pubmed:author | pubmed-author:CoubesPhilipp... | lld:pubmed |
pubmed-article:17961983 | pubmed:author | pubmed-author:CrespelAriell... | lld:pubmed |
pubmed-article:17961983 | pubmed:author | pubmed-author:GelissePhilip... | lld:pubmed |
pubmed-article:17961983 | pubmed:author | pubmed-author:GonzalezVicto... | lld:pubmed |
pubmed-article:17961983 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17961983 | pubmed:volume | 77 | lld:pubmed |
pubmed-article:17961983 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17961983 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17961983 | pubmed:pagination | 165-8 | lld:pubmed |
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pubmed-article:17961983 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17961983 | pubmed:articleTitle | Senile myoclonic epilepsy of Genton: two cases in Down syndrome with dementia and late onset epilepsy. | lld:pubmed |
pubmed-article:17961983 | pubmed:affiliation | Epilepsy Unit, Montpellier, France. | lld:pubmed |
pubmed-article:17961983 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17961983 | pubmed:publicationType | Case Reports | lld:pubmed |