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Magnetoencephalography in West syndrome

Background: Localized lesions induce West syndrome (WS), and patients with West syndrome often subsequently develop focal seizures. Methods: We evaluated patients with West syndrome using magnetoencephalography (MEG). Fourteen patients who currently or previously had West syndrome were examined at 3...

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Bibliographic Details
Published in:International Congress series 2002-04, Vol.1232, p.681-685
Main Authors: Hattori, Hideji, Matsuoka, Osamu, Morimoto, Kyoko, Seto, Toshiyuki, Yamano, Tsunekazu, Tsutada, Tuyoshi, Tsuyuguchi, Naohiro, Tanaka, Katsuji, Kawawaki, Hisashi, Shimogawara, Masahiro, Haruta, Yasuhiro
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Language:English
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Summary:Background: Localized lesions induce West syndrome (WS), and patients with West syndrome often subsequently develop focal seizures. Methods: We evaluated patients with West syndrome using magnetoencephalography (MEG). Fourteen patients who currently or previously had West syndrome were examined at 3 months to 6 years of age. MEGs were recorded using the 160-channel, whole-head, laying-type MEG system. Equivalent current dipoles were estimated at the time of spikes on the EEG. Results: The patients were classified according to MRI findings. Seven patients were in the focal lesion group (group F) and seven in the non-focal lesion group (group N). Dipoles were distributed over a wide brain area in seven patients (pattern W). Three patients had dipoles distributed over a wide area along with a dense dipole distribution in a specific cortical area (pattern WC). Four patients had a closed dipole distribution in a unilateral cerebral focal area (pattern C). Dipoles were distributed widely over the bilateral cerebral cortex in patients with infantile spasms with hypsarrhythmia. Conclusions: The change in the dipole distribution pattern in the MEG of patients with West syndrome correlated with the seizure type.
ISSN:0531-5131
1873-6157
DOI:10.1016/S0531-5131(01)00702-6