- •Preface
- •Transient Binocular Visual Loss
- •Migraine with Typical Visual Aura
- •Congenitally Elevated Optic Disc
- •Optic Disc Coloboma
- •Optic Pit
- •Morning Glory Optic Disc Anomaly
- •Optic Disc Hypoplasia
- •Typical Optic Neuritis
- •Atypical Optic Neuritis
- •Arteritic Anterior Ischemic Optic Neuropathy
- •Posterior Ischemic Optic Neuropathy
- •Hypotensive Ischemic Optic Neuropathy
- •Toxic Optic Neuropathy
- •Dominantly Inherited Optic Neuropathy
- •Leber Hereditary Optic Neuropathy
- •Sphenoid Meningioma
- •Optic Nerve Sheath Meningioma
- •Craniopharyngioma
- •Pituitary Adenoma
- •Optic Glioma (Pilocytic Astrocytoma of Optic Nerves or Chiasm)
- •Anterior Visual Pathway Intracranial Aneurysm
- •Traumatic Optic Neuropathy
- •Radiation Optic Neuropathy
- •Graves Optic Neuropathy
- •Papilledema
- •Hypertensive Optic Neuropathy
- •Paraneoplastic Optic Neuropathy
- •Diabetic Papillopathy
- •Homonymous Hemianopia
- •Cerebral (Retrogeniculate, Cortical) Blindness
- •Visual Agnosia
- •Visual Spatial And Attentional Disturbances
- •Orbital Myositis
- •Graves Disease
- •Genetic Extraocular Myopathy
- •Myasthenia Gravis
- •Third Cranial Nerve Palsy
- •Fourth Cranial Nerve Palsy
- •Sixth Cranial Nerve Palsy
- •Unilateral Ophthalmoplegia
- •Bilateral Ophthalmoplegia
- •Direct Carotid–cavernous Fistula
- •Indirect (Dural) Carotid–cavernous Fistula
- •Internuclear Ophthalmoplegia
- •Skew Deviation
- •Dorsal Midbrain (Pretectal) Syndrome
- •Paramedian Thalamic or Midbrain Syndrome
- •Paramedian Pontine Syndrome
- •Dorsolateral Medullary (Wallenberg) Syndrome
- •Acute Upgaze Deviation
- •Acute Downgaze Deviation
- •Omnidirectional Slow Saccades
- •Omnidirectional Saccadic Pursuit
- •Congenital Ocular Motor Apraxia
- •Acute Horizontal Gaze Deviation
- •Ping Pong Gaze
- •Physiologic Nystagmus
- •Congenital Motor Nystagmus
- •Congenital Sensory Nystagmus
- •Monocular Pendular Nystagmus of Childhood
- •Spasmus Nutans
- •Peripheral Vestibular Nystagmus
- •Acquired Binocular Pendular Nystagmus
- •Sidebeat, Upbeat, and Downbeat Nystagmus
- •Epileptic Nystagmus
- •Convergence–retraction “Nystagmus”
- •Voluntary “Nystagmus”
- •Superior Oblique Myokymia
- •Square Wave Jerks
- •Ocular Flutter and Opsoclonus
- •Ocular Dysmetria
- •Ocular Bobbing
- •Tonic Pupil
- •Argyll Robertson Pupils
- •Tectal (Dorsal Midbrain) Pupils
- •Pharmacologically Dilated Pupil
- •Mydriatic Pupil of Third Cranial Nerve Palsy
- •Mydriatic Pupil of Traumatic Iridoplegia
- •Episodic Pupil Dilation
- •Horner Syndrome
- •Ptosis
- •Lid Retraction
- •Apraxia of Eyelid Opening
- •Benign Essential Blepharospasm
- •Hemifacial Spasm
- •Index
• 9 SECTIONDisorders Gaze Cerebral
Ping Pong Gaze
Key Facts
•Arrhythmic slow conjugate horizontal movement of the eyes from one side to the other in a comatose patient
•Caused by severe ischemic or metabolic insult to both cerebral hemispheres
•Damaged cerebral hemispheres cannot control pontine gaze generators, which discharge automatically to move eyes back and forth
•Often mistaken for epileptic nystagmus
Clinical Findings
•Conjugate horizontal eye movements taking about 5 s to complete full cycle
•Patient typically unresponsive except to painful tactile stimuli
Ancillary Testing
•CT or MRI may show extensive damage to both cerebral hemispheres
•Normal MRI suggests metabolic or toxic damage, which may be shown with blood and urine tests
Differential Diagnosis
• Epileptic nystagmus
Treatment
• Directed at underlying disorder
Prognosis
•Irreversible if ischemic damage
•May be reversible if metabolic damage
164
Fig. 9.7 Ping pong gaze. The eyes drift conjugately from one side to another. There are no volitional eye movements because the patient is in coma.
Gaze Pong Ping
Fig. 9.8 Hypoxic–ischemic encephalopathy from strangulation. Diffusion-weighted MRI shows high signal involving the cerebral cortex and basal gray matter.
165
Section |
|
|
10 |
|
|
Nystagmus |
|
|
Physiologic Nystagmus |
168 |
|
Congenital Motor Nystagmus |
170 |
|
Congenital Sensory Nystagmus |
172 |
|
Monocular Pendular Nystagmus of Childhood |
174 |
|
Spasmus Nutans |
176 |
|
Peripheral Vestibular Nystagmus |
178 |
|
Acquired Binocular Pendular Nystagmus |
180 |
|
Sidebeat, Upbeat, and Downbeat Nystagmus |
182 |
|
Epileptic Nystagmus |
186 |
|
“Nystagmus” Of Extraocular Muscle Dysfunction |
188 |
|
Convergence–retraction “Nystagmus” |
190 |
|
Voluntary “Nystagmus” |
192 |
|
|
|
|
• 10 SECTION Nystagmus
Physiologic Nystagmus
Key Facts
•Horizontal or horizontal–torsional jerk nystagmus at extremes of horizontal gaze to both sides that is considered a variant of normal function
•Often confused with pathologic nystagmus but usually distinguishable by noting clinical findings
Clinical Findings
•Fast phase in direction of gaze
•Nystagmus amplitude is low and equal in amplitude in both directions of gaze
•Nystagmus amplitude may be greater in abducting than in adducting eye
•Nystagmus stops after four or fewer beats (unsustained)
•No oscillopsia during the nystagmus
•No nystagmogenic medications or drugs
•No other pertinent abnormalities on examination
Ancillary Testing
• All tests normal (but not necessary)
Differential Diagnosis
•Congenital nystagmus
•Sidebeat nystagmus
Treatment
• None
Prognosis
• Nystagmus may appear on some examinations and not on others
168
Fig. 10.1 Physiologic nystagmus. In extremes of horizontal gaze, there is a lowamplitude jerk nystagmus with the fast component in the direction of gaze.
Nystagmus Physiologic
169
