Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report

Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease with no effective therapy available. We recorded spontaneous magnetoencephalography and auditory evoked fields (AEFs) from a male patient with a rapidly progressive memory disorder, ataxia and myoclonus. Post-mortem examination conf...

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Main Authors: Juha Wilenius, Jyrki P. Mäkelä, Jukka Lyytinen, Anders Paetau, Maarit Palomäki, Eero Pekkonen
Format: Article
Language:English
Published: Karger Publishers 2010-10-01
Series:Case Reports in Neurology
Subjects:
Online Access:http://www.karger.com/Article/FullText/321349
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spelling doaj-fa6584fd0de1462db86069a7e4429df12020-11-24T20:53:53ZengKarger PublishersCase Reports in Neurology1662-680X2010-10-012312212710.1159/000321349321349Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case ReportJuha WileniusJyrki P. MäkeläJukka LyytinenAnders PaetauMaarit PalomäkiEero PekkonenCreutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease with no effective therapy available. We recorded spontaneous magnetoencephalography and auditory evoked fields (AEFs) from a male patient with a rapidly progressive memory disorder, ataxia and myoclonus. Post-mortem examination confirmed sporadic CJD. Sources of the abnormal slow wave activity were localized with a beamformer software. Sources of sharp transients and AEFs were modeled with equivalent current dipoles. The estimated sources of spontaneous activity abnormalities were more dominant in the left hemisphere, in line with left-dominant abnormalities in diffusion-weighted MRI. Sources of AEFs were found in both temporal lobes. Magnetoencephalography measurements on CJD patients are feasible, and provide efficient means for localizing abnormal cortical activity in CJD.http://www.karger.com/Article/FullText/321349Creutzfeldt-Jakob diseasePrion diseaseTransmissible spongiform encephalopathyMagnetoencephalography
collection DOAJ
language English
format Article
sources DOAJ
author Juha Wilenius
Jyrki P. Mäkelä
Jukka Lyytinen
Anders Paetau
Maarit Palomäki
Eero Pekkonen
spellingShingle Juha Wilenius
Jyrki P. Mäkelä
Jukka Lyytinen
Anders Paetau
Maarit Palomäki
Eero Pekkonen
Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
Case Reports in Neurology
Creutzfeldt-Jakob disease
Prion disease
Transmissible spongiform encephalopathy
Magnetoencephalography
author_facet Juha Wilenius
Jyrki P. Mäkelä
Jukka Lyytinen
Anders Paetau
Maarit Palomäki
Eero Pekkonen
author_sort Juha Wilenius
title Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
title_short Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
title_full Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
title_fullStr Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
title_full_unstemmed Magnetoencephalographic Abnormalities in Creutzfeldt-Jakob Disease: A Case Report
title_sort magnetoencephalographic abnormalities in creutzfeldt-jakob disease: a case report
publisher Karger Publishers
series Case Reports in Neurology
issn 1662-680X
publishDate 2010-10-01
description Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease with no effective therapy available. We recorded spontaneous magnetoencephalography and auditory evoked fields (AEFs) from a male patient with a rapidly progressive memory disorder, ataxia and myoclonus. Post-mortem examination confirmed sporadic CJD. Sources of the abnormal slow wave activity were localized with a beamformer software. Sources of sharp transients and AEFs were modeled with equivalent current dipoles. The estimated sources of spontaneous activity abnormalities were more dominant in the left hemisphere, in line with left-dominant abnormalities in diffusion-weighted MRI. Sources of AEFs were found in both temporal lobes. Magnetoencephalography measurements on CJD patients are feasible, and provide efficient means for localizing abnormal cortical activity in CJD.
topic Creutzfeldt-Jakob disease
Prion disease
Transmissible spongiform encephalopathy
Magnetoencephalography
url http://www.karger.com/Article/FullText/321349
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