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89 Cards in this Set

  • Front
  • Back
Cogan's dictum for homonomous hemianopia
asymmetric OKN indicates parietal lobe lesion, symmetric OKN indicates occipital lobe lesion
CN most prone to injury in cavernous sinus
CN 6
lesion location in seesaw nystagmus
suprasellar lesion
ipsilateral Horner's syndrome and contralateral CN4 palsy
midbrain lesion
OKN strip moved to the left stimulates
right frontal, left occipital
horizontal gaze center: smooth pursuit
- ipsilateral parieto-occipital lobe to superior colliculus to PPRF to horizontal gaze center (CN6 nucleus) to ipsilateral LR and contralateral MR via MLF (medial longitudinal fasciculus)
vertical smooth pursuit
interstitial nucleus of Cajal
horizontal smooth pursuit
ipislateral parieto-occipital lobe
speed of smooth pursuit
slow eye movements
horizontal gaze center: saccades
contralateral frontal eye fields (frontal lobe) to superior colliculus to pintine paramedian reticular formation (PPRF) to horizontal gaze center (CN6 nucleus) to ipislateral LR and cotnralateral MR via medial longitudinal fasciculus (MLF)
Vergence system
frontal and occipital lobes and midbrain
horizontal gaze center: saccades
contralateral frontal eye fields (frontal lobe) to superior colliculus to pontine paramedian reticular formation to horizontal gaze center (CN6 nucleus) to ipsilateral LR and contralateral MR via MLF
One and a half syndrome
- Fisher syndrome
- CN6 nucleus and ipsilateral MLF
- causes ipsilateral gaze palsy and INO
- only movement is abduction of contralateral eye with nystagmus
downbeat nystagmus
- lesions that affect pathway for downgaze
- cervicomedullary junction
- spinocerebellar degeneration
- lithium
upbeat nystagmus
- medullary lesion
- midline cerebellar (vermis) lesions
- MS
ocular bobbing
- rapid downward movements followed by slow return to primary position
- secondary to hemorrhage
- comatose patient
ocular dipping
- opposite of bobbing
- intermittent rapid upward movements followed by slow return to primary
opsoclonus
- saccadomania
- dancing hands and feet
- abnormality of pause cells that normally suppress burst cells of PPRF
- remote effect on cerebellum from metastatic neuroblastoma, occasionally with encephalitis
CN6 palsy syndromes
brain stem syndromes
- Millard-Gubler: CN6 and CN7 and contralateral hemiparesis
- Raymond's: CN6 and contralateral hemiparesis
- Foville's: CN6, CN5, CN7and sympathetics
- Moebius: CN7, extra digits, mental retardation
Ramsay-Hunt syndrome
HZV of outer ear and inner autidotry canal, 20% hearing loss and dizziness
facial myokymia
if multifocal and progressive consider MS
eyelid myokymia
benign lid fasciculation
Eaton-Lambert syndrome
paraneoplastic, impaired presynaptic release of ACh, antibodies against presynaptic votage-gated Ca-channels
CHAMPS
controlled high-risk Avonex MS prevention study: 3 year risk lower and fewer MRI lesions
ONTT
optic neuritis treatment trial
30% MS at 5 years regardless of treatment (16% with no, 51% with lesions)
CN3 palsy syndromes (fascicle)
Nothnagel's: CN3 and superior cerebellar peduncle (cerebellar ataxia)
Benedikt's syndrome: CN3 and red nucleus (contralateral hemitremor and decreased sensation)
Weber's syndrome: CN3 and pyrimidal tract with contralateral hemparesis
diabetic CN3 palsy
pain possible but no aberrant regeneration
VER
not useful for distinguishing optic neuropathy form retinal disorders
lesions affecting the optic tract may be associated with
- unilaterally decreased visual acuity
- ipsilateral APD
- contralateral APD
- homonymous hemianopia
T1-weighted images
renerated by short repetition times (TR) and short echo times (TE)
life-expectancy in CRAO
same
Percentage of MS patients who will develop optic neuritis?
55%
Percentage of patients with severe MS and optic neuritis on autopsy?
100%
Percentage of pts with opitc nerve glioma who have neurofibromatosis
12-38%
location of alexia with agraphia
domiant angular gyrus
location of alexia without agraphia
occipital lobe and corpus callosum
location of cerebral dyschromatopsia
unilateral or bilateral inferior occipitotemporal junction
location of unformed hallucinations
bialteral inferior occipitotemporal junction
6th nerve palsy due to intracavernous lesion
- may present as abduction palsy plus miosis
- in cavernous sinus, sympathetic branches of the paracarotid plesux joins the 6th nerve briefly
first saccadic movement to be affected in progressive supranuclear palsy
downward
latency in generating a pursuit movement
shorter than that for a saccade
dorsal midbrain syndrome associated with
- upward gaze paresis
- accommodative abnormalities
- light-near dissociation
- lid retraction
- NOT: paradoxic OKN
Percentage of patients with Bell's palsy with complete spontaneous recovery
75%
cranial nerve most frequently involved in neurosarcoidosis
1st: CN7, 2nd CN2
pathway for accomodative miosis
enters Edinger-Westphal nucleus anterior to the pathway for light-induced miosis
most common etiology of doral midbrain syndrome in child under 10 years of age
pineal gland tumor
pupillary dilation only sign of CN3 palsy in which disorders
- uncal herniation
- basilar meningitis
most commonly motor nerve affected in MS
CN6
chronic sinopulmonary infections seen as part of what phacomatosis
ataxia-teleangiectasia
most frequently involved extraocular msucle in Graves ophthalmopathy
- 1st inferior rectus
- 2nd medial rectus
- least frequently: lateral rectus
percentage of patients with myasthenia gravis who develop Graves disease
5%
percentage of patients with myasthenia gravis who develop thymoma
10%
cues to presence of high-grade carotid stenosis
- low-grade anterior segment inflammation
- cataract
- hypotony
- contralateral corneal arcus
neurologic association with Coats disease
- facioscapulohumeral dystrophy
- Turner's syndrome
- Senir-Loken syndrome
- epidermal nevus syndrome
releave downbeat nystagmus in Arnold-Chiari
- clonazepam
- basilar craniectomy
Parinauds dorsal midbrain syndrome
pinealoma
differential for presumed posterior ischemic optic neuropathy
- radiation optic neuropathy
- post-coronary artery bypass graft surgery
- giant cell arteritis
meningioma arising in which location is most likey to lead to opitic disc edema
optic nerve sheath (must be 1 cm or closer)
skew deviation
vertical misalignment of visual axes due to imbalance of prenuclear inputs
brain stem infarct, MS, high ICP, vertebral basilar insufficiency
diabetic papillopathy
- vision loss mild
- independent of degree of BS control
sudden severe headache with accompanying acute visual loss is a well-recognized compolication of
pituitary adenoma
tropia pattern in bilateral 4th nerve palsy
V pattern esotropia
brainstem nuclei critical for generation of normal vertical eye movements
- rostral interstitial nucleus of medial longitudinal fasciculus
- interstitial nucleus of Cajal
bilateral INO
more common in demyelinating disease (perfusion respects midline)
brainstem lesion that involves both medial longitudinal fasciculi near their junctions with the third nerve nuclei may cause
walleyed bilateral INO
Variant of Guillain-Barre syndrome that only involves the brainstem and cranial nerves
Fisher syndrome
prevalence of giant cell arteritis in above 50 yos
1 in 75.000
1% in above 90 yo
prevalence of polymyalgia rheumatica over 50 yo
1 in 200
parasympathetic fibers destined for pupil reside in
medial portion of CN3
lesion of left occipital lobe
may show monocular right temporal visual feild defect
aberrant regeneration
never seen after vascular lesion
laterality of facial spasm
- hemifacial spasm unilateral 90-95%
- blepharospasm always bilateral but may be asymmetric
Parks-Bielschowsky 3-step test
1. Which eye is hyperopic?
LH: paresis of OD elevators (RSR or RIO) or OS deressors (LIR or LSO)
2. Worse on right or left gaze?
If hyper, is wore in left gaze: OS muscles with greatest vertical action during abduction (SR and IR); OD muscles that have greatest vertical action during adduction (SO and IO)
SR and IR best in ABduction: if left hyper worse on left gaze: LIR
SO and IO best in ADduction: if left hyper worse on left gaze: RIO
if LH worse on right gaze: RSR or LSO
3. Worse on right or left tilt? If 1 of the intorters is cause then will worsen hyper on side of head tilt
If worse hyper on left head tilt, problem with left intorters (LSRR, LSO) or right extorters (RIR, RIO)
ocular myasthenia gravis
antibodies only found in less than 60%
less than 20% chance of systemic MG
CN6 nucleus lesion and gaze palsy
gaze palsy to same side (nucleus has interneurons destined for the contralateral medial rectus subnucleus via the MLF/medial longitudinal fasciculus)
muscles innervated by crossed projections
superior rectus (subnucleus), superior oblique
superior orbital fissure
CN3, 4, 5/1, 6
Benedikt's syndrome
CN3 palsy, contralateral decreased sensation, contralateral tremor
optokinetic reflex drum rotating left and left VF defect
acutely ipsilateral pursuit affected
cocaine
inhibits reuptake of norepinephrine; no dilation in Horners because no NE present (only works if all 3 neurons are intact)
amphetamine
cause release of NE (only works if 3rd neuron intact)
parasympathetic fibers to lacrimal gland synapse in which ganglion
sphenopalatine
Bourneville's
tuberous sclerosis
Sturge-Weber
encephalo-trigeminal angiomatosis
von Hippel-Lindau
angiomatosis retinae
psammoma bodies
ON meningioma
von Recklinghausen
neurofibromatosis
Louis-Bar
ataxia-telangiectasia