Cerebellar Dysfunction Flashcards

1
Q

possible causes of cerebellar dysfunction

A

stroke
tumor
chiari malformation
toxicity
trauma
infection
immune mediated
endocrine
multiple systems artophy
idiopathic ataxia
hereditary disorders

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2
Q

what cerebellar dysfunction has an acute/abrupt onset

A

CVA, brain lesions

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3
Q

what cerebellar dysfunction has a rapid progression

A

infarction, immune-mediated disorders

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4
Q

what cerebellar dysfunction has a slower progression

A

paraneoplastic disorders
encephalopathy
vit d deficiency
general med conditions

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5
Q

what cerebellar dysfunction has a chronic progression

A

genetic ataxias
toxins

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6
Q

primary dx for cerebellar dysfunction

A

brain and brainstem MRI

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7
Q

SxS of alcholic ataxia

A

wide footed gait, unsteady
dysarthria
clumsiness of their hands
diplopia, saccades
peripheral neuropathy

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8
Q

wernicke-koraskoff syndrome

A

chronic alcohol use – thiamine (vit B1) deficiency

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9
Q

korsakoff’s psychosis

A

severe impairments in immediate recall
anterograde or retrograde amnesia
disorientation
emotional changes
confabulation

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10
Q

wernicke’s encephalitis

A

confusion
ataxia
opthalmoplegia
anisocoria
nystagmus

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11
Q

chiari malformation

A

congenital condition in which structural abnormalities lead to herniation of cerebellum through foramen magnum, compressing involved structures

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12
Q

type 1 chiari malformation

A

symptoms appear in adolescense or adulthood

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13
Q

type 2 chiari malformation

A

symptoms appear in childhood, more severe than type 1

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14
Q

type 3 chiari malformation

A

rare, most severe, seen in babies

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15
Q

symptoms of chiari malformation

A

neck pain
occipital HA
hearing/balance problems
dizziness
vomiting
tinnitus
incoordination

can be asymptomatic

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16
Q

treatment for asymptomatic chiari malformation

A

monitor

17
Q

treatment for symptomatic chiari malformation

A

surgery - posterior fossa decompression

18
Q

friedreich’s ataxia

A

hereditary ataxia

degeneration of spinal and peripheral nerves
onset in childhood

19
Q

SxS of friedreich’s ataxia

A

imbalance, incoordination, dysarthria, dysphagia, weakness

scoliosis, visual/hearing loss, hypertrophic cardiomyopathy, peripheral neuropathy

20
Q

prognosis of friedreich’s ataxia

A

mortality between 40-60s

21
Q

what is the common cause of death for friedreich’s ataxia

A

heart disease

22
Q

spinocerebellar ataxia

A

hereditary ataxia

degenerative process involving cerebellum and its efferent and afferent connections

23
Q

spinocerebellar ataxia may affect what

A

basal ganglia
brainstem nuclei
pyramidal tracts
spinal cord
alpha MNs

24
Q

spinocerebellar ataxia prognosis

A

unknown

25
Q

spinocerebellar ataxia type 1

A

optic atrophy, opthalmoplegia, dementia, amyotrophy, extrapyramidal signs

26
Q

spinocerebellar ataxia type 2

A

retinal degeneration, which may be associated with opthalmoplegia and extrapyramidal signs

27
Q

spinocerebellar ataxia type 3

A

pure cerebellar ataxia

28
Q

spinocerebellar ataxia type 4

A

deafness and presence of myoclonus

29
Q

what is the SARA

A

scale for assessment and rating ataxia

30
Q

what does the SARA evaluate

A

gait, standing, sitting, speech, finger to nose, nose to finger, RAMs, heel to shin

31
Q

what does the SARA not consider

A

oculomotor function

32
Q

what is the SARA scale

A

0 no ataxia
40 most severe ataxia