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
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 KOEPPEN, A. H.
Right arrow Articles by HANS, M. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by KOEPPEN, A. H.
Right arrow Articles by HANS, M. B.
NEUROLOGY 1976;26:764
© 1976 American Academy of Neurology

Supranuclear ophthalmoplegia in olivopontocerebellar degeneration

ARNULF H. KOEPPEN, M.D. and MARY B. HANS, M.S.W.

From the Neurology Service, Veterans Administration Hospital, and the Department of Neurology, Albany Medical College, Albany, New York.

Autosomal dominant olivopontocerebellar degeneration was diagnosed in a family of Scottish ancestry by clinical examination and autopsy. In addition to having progressive cerebellar ataxia, head titubation, and severe dysarthria, the patients are unable to initiate saccadic eye movements. Slow pursuit movements are normal. Reflex movements of the eyes caused by passive rotation or caloric labyrinthine stimulation are not impaired but are not associated with nystagmus. The phenomenon can be classified as supranuclear pseudo-ophthalmoplegia. It differs from congenital ocular motor apraxia in age at onset and the absence of random eye movements. The anatomic lesion responsible for the defect of saccadic eye movements remains to be established.

Reprint requests should be addressed to Dr. Koeppen, Neurology Service, Veterans Administration Hospital, Albany, NY 12208.

Dr. Koeppen was the recipient of a travel grant from the Veterans Administration, Washington, DC.

Received for publication August 28, 1975.




This article has been cited by other articles:


Home page
Arch NeurolHome page
A. H. Koeppen, P. Coutinho, and C. Barbot
Ocular Apraxia in Recessive Ataxia
Arch Neurol, May 1, 2002; 59(5): 874 - 874.
[Full Text] [PDF]


Home page
Arch NeurolHome page
K. Wessel, C. Moschner, K.-P. Wandinger, D. Kompf, and W. Heide
Oculomotor Testing in the Differential Diagnosis of Degenerative Ataxic Disorders
Arch Neurol, July 1, 1998; 55(7): 949 - 956.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1976 by AAN Enterprises, Inc.