Source:http://linkedlifedata.com/resource/pubmed/id/19128987
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2009-4-6
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pubmed:abstractText |
Malformations of cortical development (MCD) encompass a wide spectrum of brain disorders. Although rare, the combination of certain MCD may occur. We report a rare case of combination of three distinct cerebral pathologies: tuberous sclerosis, polymicrogyria and hippocampal sclerosis in a patient with intractable epilepsy. Ictal EEG and ictal SPECT suggested right perisylvian area as a seizure onset zone. However, on MRI multiple potentially epileptogenic lesions were identified. The neurobiological background of the coexistence of different types of malformations of cortical development remains enigmatic.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1059-1311
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
303-5
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pubmed:meshHeading |
pubmed-meshheading:19128987-Cerebral Cortex,
pubmed-meshheading:19128987-Electroencephalography,
pubmed-meshheading:19128987-Female,
pubmed-meshheading:19128987-Hippocampus,
pubmed-meshheading:19128987-Humans,
pubmed-meshheading:19128987-Magnetic Field Therapy,
pubmed-meshheading:19128987-Malformations of Cortical Development,
pubmed-meshheading:19128987-Tomography, Emission-Computed, Single-Photon,
pubmed-meshheading:19128987-Tuberous Sclerosis,
pubmed-meshheading:19128987-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
Tuberous sclerosis complex with unilateral perisylvian polymicrogyria and contralateral hippocampal sclerosis - a case report.
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pubmed:affiliation |
Department of Neurology, Innsbruck Medical University, Anichstrasse 35, A-6020 Innsbruck, Austria. raimund.helbok@uki.at
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pubmed:publicationType |
Journal Article,
Case Reports
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