CN, cerebellar and atlas/axis disorders Flashcards

1
Q

facial nerve paralysis

A

unilateral, ear drop, inability to close the eye, keratitis, muzzle pulled to unaffected side

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2
Q

peripheral vestibular disease

A

CN VIII or vestibular apparatus damaged

clinical signs: head tilt, ataxia, drifting to one side, horizontal nystagmus

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3
Q

vestibular disease dx

A

skull rads, titers for protozoal myelitis

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4
Q

central vestibular disease etiology

A

head trauma, stylohyoid osteoarthropathy, pathologic fx extends into petrous temporal bone, EPM

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5
Q

central vestibular disease clinical signs

A

vestibular sxs

additional CN V through XII involvement

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6
Q

temorohypoid osteoarthropathy

A

CN VII, VIII deficits

central corneal ulcer

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7
Q

tx of vestibular disease

A

antiinflammatory drugs-DMSO, corticosteroids, NSAIDs
abx-TMPS for otitis, pen/gent for skull fx
surgery

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8
Q

guttural pouch empyema

A

involve facial, vagus, and glossopharyngeal nerves and cranial sympathetic trunk

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9
Q

guttural pouch mycosis

A

hemorrhage

dysfunction of CN VII, IX, X, XI

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10
Q

dysphagia

A

brainstem nuclear regions, glossopharyngeal and vagus nerves

severe forebrain diseases-swallowing reflexes are still intact

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11
Q

ddx of dysphagia

A

inflammatory
toxic
physical
non-neurologic

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12
Q

cerebellar disease

A
ataxia without weakness
dysmetric
jerky head bobbing
intention tremor
absent or inconsistent menace
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13
Q

cerebellar abiotrophy

A

arabian foals

signs develop at 1-6 months of age

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14
Q

cerebellar abiotrophy pathogenesis

A

autosomal recessive genetic basis

degeneration and depletion of Purkinje and granular cells

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15
Q

cerebellar hypoplasia

A

associated with BVD infection
clinical signs apparent at birth
small cerebellum

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16
Q

occipitoatlantoaxial malformation

A

familial occipitalizatin of the atlax with atlantalization of axis
arabian, friesian, saddlebred, appaloosa
3 clinical presentations: dead at birth, tetraparesis at birth, progressive ataxia in foals