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A Case of Hunt Syndrome with Laryngeal Paralysis Satoshi Kawai 1 1Department of Otorhinolaryngology, Yokohama Sakae Kyosai Hospital pp.951-956
Published Date 1993/11/20
DOI https://doi.org/10.11477/mf.1411900834
  • Abstract
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A 78-year-old female with Hunt syndrome developed cranial polyneuritis, such as peripheral facial palsy, dizziness, swallowing disturbance and left laryngeal paralysis. The disturbance of cranial nerves was disappeared completely by intravenous infusion of Vidarabine.

We discussed 32 cases of Hunt syndrome with cranial polyneuritis in previous reports.


Copyright © 1993, 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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