CN, cerebellar and atlas/axis disorders Flashcards
facial nerve paralysis
unilateral, ear drop, inability to close the eye, keratitis, muzzle pulled to unaffected side
peripheral vestibular disease
CN VIII or vestibular apparatus damaged
clinical signs: head tilt, ataxia, drifting to one side, horizontal nystagmus
vestibular disease dx
skull rads, titers for protozoal myelitis
central vestibular disease etiology
head trauma, stylohyoid osteoarthropathy, pathologic fx extends into petrous temporal bone, EPM
central vestibular disease clinical signs
vestibular sxs
additional CN V through XII involvement
temorohypoid osteoarthropathy
CN VII, VIII deficits
central corneal ulcer
tx of vestibular disease
antiinflammatory drugs-DMSO, corticosteroids, NSAIDs
abx-TMPS for otitis, pen/gent for skull fx
surgery
guttural pouch empyema
involve facial, vagus, and glossopharyngeal nerves and cranial sympathetic trunk
guttural pouch mycosis
hemorrhage
dysfunction of CN VII, IX, X, XI
dysphagia
brainstem nuclear regions, glossopharyngeal and vagus nerves
severe forebrain diseases-swallowing reflexes are still intact
ddx of dysphagia
inflammatory
toxic
physical
non-neurologic
cerebellar disease
ataxia without weakness dysmetric jerky head bobbing intention tremor absent or inconsistent menace
cerebellar abiotrophy
arabian foals
signs develop at 1-6 months of age
cerebellar abiotrophy pathogenesis
autosomal recessive genetic basis
degeneration and depletion of Purkinje and granular cells
cerebellar hypoplasia
associated with BVD infection
clinical signs apparent at birth
small cerebellum