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dc.contributor.authorHunold, Alexanderen_US
dc.contributor.authorHaueisen, Jensen_US
dc.contributor.authorAhtam, Banuen_US
dc.contributor.authorDoshi, Chiranen_US
dc.contributor.authorHarini, Chellamanien_US
dc.contributor.authorCamposano, Susanaen_US
dc.contributor.authorWarfield, Simon K.en_US
dc.contributor.authorGrant, Patricia Ellenen_US
dc.contributor.authorOkada, Yoshioen_US
dc.contributor.authorPapadelis, Christosen_US
dc.date.accessioned2014-05-06T16:18:33Z
dc.date.issued2014en_US
dc.identifier.citationHunold, Alexander, Jens Haueisen, Banu Ahtam, Chiran Doshi, Chellamani Harini, Susana Camposano, Simon K. Warfield, Patricia Ellen Grant, Yoshio Okada, and Christos Papadelis. 2014. “Localization of the Epileptogenic Foci in Tuberous Sclerosis Complex: A Pediatric Case Report.” Frontiers in Human Neuroscience 8 (1): 175. doi:10.3389/fnhum.2014.00175. http://dx.doi.org/10.3389/fnhum.2014.00175.en
dc.identifier.issn1662-5161en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:12153028
dc.description.abstractTuberous sclerosis complex (TSC) is a rare disorder of tissue growth and differentiation, characterized by benign hamartomas in the brain and other organs. Up to 90% of TSC patients develop epilepsy and 50% become medically intractable requiring resective surgery. The surgical outcome of TSC patients depends on the accurate identification of the epileptogenic zone consisting of tubers and the surrounding epileptogenic tissue. There is conflicting evidence whether the epileptogenic zone is in the tuber itself or in abnormally developed surrounding cortex. Here, we report the localization of the epileptiform activity among the many cortical tubers in a 4-year-old patient with TSC-related refractory epilepsy undergoing magnetoencephalography (MEG), electroencephalography (EEG), and diffusion tensor imaging (DTI). For MEG, we used a prototype system that offers higher spatial resolution and sensitivity compared to the conventional adult systems. The generators of interictal activity were localized using both EEG and MEG with equivalent current dipole (ECD) and minimum norm estimation (MNE) methods according to the current clinical standards. For DTI, we calculated four diffusion scalar parameters for the fibers passing through four ROIs defined: (i) at a large cortical tuber identified at the right quadrant, (ii) at the normal appearing tissue contralateral to the tuber, (iii) at the cluster formed by ECDs fitted at the peak of interictal spikes, and (iv) at the normal appearing tissue contralateral to the cluster. ECDs were consistently clustered at the vicinity of the large calcified cortical tuber. MNE and ECDs indicated epileptiform activity in the same areas. DTI analysis showed differences between the scalar values of the tracks passing through the tuber and the ECD cluster. In this illustrative case, we provide evidence from different neuroimaging modalities, which support the view that epileptiform activity may derive from abnormally developed tissue surrounding the tuber rather than the tuber itself.en
dc.language.isoen_USen
dc.publisherFrontiers Media S.A.en
dc.relation.isversionofdoi:10.3389/fnhum.2014.00175en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972469/pdf/en
dash.licenseLAAen_US
dc.subjectelectroencephalographyen
dc.subjectepileptogenic zoneen
dc.subjectequivalent current dipoleen
dc.subjectmagnetoencephalographyen
dc.subjectpediatric epilepsyen
dc.subjecttuberous sclerosis complexen
dc.titleLocalization of the Epileptogenic Foci in Tuberous Sclerosis Complex: A Pediatric Case Reporten
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalFrontiers in Human Neuroscienceen
dash.depositing.authorAhtam, Banuen_US
dc.date.available2014-05-06T16:18:33Z
dc.identifier.doi10.3389/fnhum.2014.00175*
dash.contributor.affiliatedCamposano, Susana
dash.contributor.affiliatedHarini, Chellamani
dash.contributor.affiliatedPapadelis, Christos
dash.contributor.affiliatedOkada, Yoshio
dash.contributor.affiliatedAhtam, Banu
dash.contributor.affiliatedWarfield, Simon


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