Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Keane, MD, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Keane, MD, J. R.
NEUROLOGY 1990;40:684
© 1990 American Academy of Neurology

The pretectal syndrome

206 patients

James R. Keane, MD

Department of Neurology, Los Angeles County/University of Southern California Medical Center, Los Angeles, CA.

The pretectal syndrome occurred in 2.3% of patients personally examined over an 18-year period. The symptoms were nonspecific, but the signs (abnormal pupils in 198 patients, vertical gaze limitation in 180, disjunctive horizontal eye position in 90 and vertical in 79, lid retraction in 83, and convergence-retraction nystagmus in 71) were exquisitely localizing. The etiology, skewed by the local prevalence of cysticercosis, was hydrocephalus in 80 patients, stroke in 53, and tumor in 45. The importance of timely diagnosis was underscored by the relatively good prognosis of many patients.

Address correspondence and reprint requests to Dr. James R. Keane, 1200 North State Street, Los Angeles, CA 90033.

Received July 10, 1989. Accepted for publication in final form September 1, 1989.




This article has been cited by other articles:


Home page
Br. J. Ophthalmol.Home page
N R Miller
Late improvement in upward gaze in a patient with hydrocephalus related Parinaud dorsal midbrain syndrome
Br. J. Ophthalmol., January 1, 2006; 90(1): 123 - 123.
[Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
G D Perkin
Neuro-ophthalmological syndromes for neurologists
J. Neurol. Neurosurg. Psychiatry, December 1, 2004; 75(suppl_4): iv20 - iv23.
[Full Text] [PDF]


Home page
Mult SclerHome page
E. M Frohman, R. B Dewey, and T. C Frohman
An unusual variant of the dorsal midbrain syndrome in MS: clinical characteristics and pathophysiologic mechanisms
Multiple Sclerosis, June 1, 2004; 10(3): 322 - 325.
[Abstract] [PDF]


Home page
Arch NeurolHome page
K.-D. Choi, D. S. Jung, and J. S. Kim
Specificity of "Peering at the Tip of the Nose" for a Diagnosis of Thalamic Hemorrhage
Arch Neurol, March 1, 2004; 61(3): 417 - 422.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
P. Pullicino, N. Lincoff, and B. T. Truax
Abnormal vergence with upper brainstem infarcts: Pseudoabducens palsy
Neurology, August 8, 2000; 55(3): 352 - 358.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
K. N. North, R. A. Ouvrier, C. A. McLean, and I. J. Hopkins
Idiopathic Hypothalamic Dysfunction With Dilated Unresponsive Pupils: Report of Two Cases
J Child Neurol, July 1, 1994; 9(3): 320 - 325.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1990 by AAN Enterprises, Inc.