Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-9pm4c Total loading time: 0 Render date: 2024-04-26T19:48:16.505Z Has data issue: false hasContentIssue false

7 - Eye movement abnormalities

from PART I - CLINICAL MANIFESTATIONS

Published online by Cambridge University Press:  17 May 2010

Charles Pierrot-Deseilligny
Affiliation:
Paul Castaigne Clinic, Pitié-Salpêtrière, Paris, France
Julien Bogousslavsky
Affiliation:
Université de Lausanne, Switzerland
Louis R. Caplan
Affiliation:
Harvard Medical School
Get access

Summary

Introduction

Eye movement commands originate in diverse cerebral hemispheric areas (for saccades and smooth pursuit) or in labyrinths (for the vestibular ocular reflex). They are carried out in the brainstem by the immediate premotor structures and the motor nuclei. Conjugate lateral eye movements are largely organized in the pons, and vertical eye movements and convergence in the midbrain. In the first part of this chapter, we will see the main types of eye movement paralysis resulting from brainstem lesions, and the related physiopathology. Such types of abnormalities are easily detected at bedside by studying three main types of eye movements: saccades, i.e. rapid eye movements made towards a visual target (such as the finger of the examiner); smooth pursuit, elicited by a small visual target moving slowly in front of the subject's eyes; the vestibular ocular reflex (VOR), tested using the oculocephalic movement, by moving passively the subject's head. In the second part of this chapter, eye movement disturbances due to cerebellar and cerebral hemispheric lesions, resulting in relatively more subtle syndromes, will be reviewed.

BRAINSTEM

Lateral eye movements

Final common pathway

The final common pathway of conjugate lateral eye movements begins in the abducens nucleus, which contains: (i) the motor neurones projecting onto the ipsilateral lateral rectus; and (ii) the internuclear neurones, which decussate at the level of the abducens nucleus, run through the medial longitudinal fasciculus (MLF) and project onto the medial rectus motor neurones in the contralateral oculomotor nucleus (Fig. 7.1) (for review, see Pierrot-Deseilligny, 1990 and Leigh & Zee, 1999).

Type
Chapter
Information
Stroke Syndromes , pp. 76 - 86
Publisher: Cambridge University Press
Print publication year: 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×