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Landau-Kleffner Syndrome:A Case Report Shin-ichiro Kitajiri 1 1Department of Otolaryngology-Head and Neck Surgery, Kyoto University Graduate School of Medicine pp.49-52
Published Date 2002/1/20
DOI https://doi.org/10.11477/mf.1411902475
  • Abstract
  • Look Inside

A 7-year-old female presented with a rapid deterio-ration of speech comprehension and expression.

She had a past history of partial seizure at age ofthree years, but her development was normal.

There were no abnormal findings in her ear drum. ABR and MRI showed no abnormal findings. Her EEG showed frequent multifocal spike-wave discharges, which became continuous when she was asleep.

The diagnosis was Landau-Kleffner syndrome. She was given γ-globlin intravenously, but the symptoms were not changed. Then, she was given corticosteroid intravenously, and her speech was recovered.


Copyright © 2002, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1316 印刷版ISSN 0914-3491 医学書院

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