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Two cases of ocular dipping Sachiko Nishida 1 , Naoki Nakano 1 , Hiroshi Ishikawa 1 , Shusaku Kitano 1 1Dep. of Ophthalmol., Nihon Univ. Sch. of Med. pp.377-380
Published Date 1985/3/15
DOI https://doi.org/10.11477/mf.1410209381
  • Abstract
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Two cases of ocular dipping are reported. One case was a 7-year-old girl with severe hypoxia due to drowning and the other was a one-year-old female baby with Lennox syndrome. Both cases manifested characteristic downward eye movements consisting of slow downward and rapid upward movements. Horizontal eye movements were intact as different from ocular bobbing.

It appeared that the ocular dipping in these cases resulted from upward gaze palsy and impairment of the inhibitory fibers involved in downward gaze. Acute hypoxia also seemed to have played a crucial role in the genesis of ocular dipping.

The clinical features and particularly the associ-ation of Lennox syndrome indicated that the lesion responsible for the abnormal eye movemets was located in the thalamo-mesencephalic junction.


Copyright © 1985, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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