You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 42 No. 8, August 1985 TABLE OF CONTENTS
  Archives
  •  Online Features
  ARTICLES
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Primary Position Upbeat Nystagmus

Localizing Value

Isao Kato, MD; Tadashi Nakamura, MD; Jin Watanabe, MD; Koji Harada, MD; Masaru Aoyagi, MD; Tadashi Katagiri, MD

Arch Neurol. 1985;42(8):819-821.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Primary position upbeat nystagmus has been associated clinically with lesions of the midbrain,1 cerebellar vermis,2-5 brachium conjunctivum,6 and lower brain stem near the inferior olive.7-9 However, only the latter two lesions have been confirmed pathologically.6-8 Even in these studies, the precise localization remains unclear. We report a case of primary position upbeat nystagmus with a discrete vascular lesion that involved the hypoglossal nucleus and and adjacent structures.

REPORT OF A CASE

A 39-year-old woman was admitted seven days after a sudden onset of dysarthria and vertical oscillopsia. Results of an examination showed primary position upbeat nystagmus that persisted in all directions of gaze. No other oculomotor abnormalities were noticed. The tongue deviated to the right; fasciculation and slight atrophy were seen on the right side of the tongue with simultaneous palatal weakness (Fig 1). No other abnormal signs were observed.

Normal laboratory studies included complete . . . [Full Text PDF of this Article]


Author Affiliations

From the Departments of Otolaryngology (Drs Kato, Nakamura, Watanabe, Harada, and Aoyagi) and Neurology (Dr Katagiri), Yamagata University School of Medicine, Yamagata, Japan.


Footnotes

Accepted for publication March 22, 1984.

Reprint requests to Department of Otolaryngology, Yamagata University School of Medicine, 990-23 Yamagata, Japan (Dr Kato).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1985 American Medical Association. All Rights Reserved.