Cranial Nerves III, IV, VI: Eye Movements

Published on 09/04/2015 by admin

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Last modified 22/04/2025

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Cranial Nerves III, IV, VI

Eye Movements

BACKGROUND

Eye movements can be divided into four types:

The sites of control of these eye movements differ (Fig. 9.1).

In the brainstem, the inputs from the frontal and occipital lobes, the cerebellum and the vestibular nuclei are integrated so that both eyes move together. Important structures are the centre for lateral gaze in the pons and the medial longitudinal fasciculus (MLF), which runs between the nuclei of the III and IV cranial nerves (in the midbrain) and the VI (in the pons).

The III, IV and VI cranial nerves then control the following muscles (Fig. 9.2):

Abnormalities can arise at any level (Fig. 9.1):

No double vision (generally):

Double vision:

Internuclear and supranuclear lesions rarely cause double vision.

WHAT TO DO

Look at the position of the head.

Look at the eyes.

Look at the position of the eyes in primary gaze.

Perform the cover test (Fig. 9.3).

The cover test

What to do

This is a test for latent squint.

Ask the patient to look with both eyes at your right eye, then cover his left eye. Then uncover the left eye rapidly and cover the right eye. Look to see if the left eye has to correct to look back at your eye. Repeat, covering the left eye and watching the right eye.

What you find

If one eye has to correct as it is uncovered, this indicates that the patient has a latent strabismus (squint), which can be classified as divergent or convergent.

Test the eye movements to pursuit

As you do this, watch the movements of the eyes.

If the patient reports seeing double at any stage:

Test convergence

Ask the patient to look into the distance and then look at your finger placed 50 cm in front of him. Gradually bring the eyes in, observing the limit of convergence of the eyes.

Vestibulo-ocular reflex (doll’s eye manœuvre)

This test is most commonly used in unconscious patients, when it provides a way of testing eye movements. In conscious patients with limited eye movements on command or pursuit, the test can be used to demonstrate preserved eye movements on vestibulo-positional stimulation, indicating a supranuclear eye movement abnormality.

Ask the patient to look into the distance at a fixed point; turn his head to the left then the right, and flex the neck and extend the neck.

The eyes should move within the orbits, maintaining forward gaze.

WHAT YOU FIND

• The eyes are misaligned in primary gaze:

– The misalignment remains constant in all directions for gaze = convergent or divergent concomitant strabismus (squint).

– One eye is deviated downwards and out, with ptosis = third nerve lesion.

– Eyes aligned in different vertical planes = skew deviation.

• The patient has double vision (Fig. 9.4):

Try to answer the following questions:

Is there a single nerve (VI, III or IV) deficit (Fig. 9.5)?

– If there is a third nerve deficit, is it medical (pupil-sparing) or surgical (with pupillary dilatation)?

If not single nerve:

– Is there a combination of single nerves?

– Is it myasthenia or dysthyroid eye disease?

• The patient does not have double vision: Compare movements on command, on pursuit and on vestibular positional testing.

WHAT IT MEANS

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Posterior communicating aneurysm is a common cause of a surgical third nerve palsy.

• Nuclear lesions: arise from brainstem pathology, including brainstem infarction, multiple sclerosis and, rarely, brainstem haemorrhage and tumour.

• Lateral gaze palsy: can arise from:

– a large frontal or parietal lobe lesion when the patient looks away from the paralysed side (can be overcome by doll’s eye manœuvre)

– a pontine lesion when the patient cannot look to the non-paralysed side and there may be other pontine abnormalities (facial weakness); not overcome using doll’s eye manœuvre.

• Vertical gaze palsy: lesions in the upper brainstem.

Common causes of lateral and vertical gaze palsies: brainstem infarction, multiple sclerosis, tumour.

• Internuclear ophthalmoplegia = a lesion to the medial longitudinal fasciculus. Common cause: multiple sclerosis. Rarer causes: vascular disease, pontine glioma.

• Supranuclear palsy with preserved positional/vestibular testing: may arise in association with akinetic rigid syndromes (Chapter 24), when it is referred to as the Steele–Richardson syndrome or progressive supranuclear palsy, and may be seen in other degenerative conditions.

• Hypometric saccades: indicate a cerebellar lesion—see Chapter 23.