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