6.5 Movement Disorders Flashcards

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1
Q
  • move too little
  • akinetic/rigid syndromes
  • parkinsonism
A

hypokinetic movement disorders

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2
Q
  • move too much

- abnormal, involuntary movements

A

hyper-kinetic movement disorders

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3
Q

primary clinical signs of Parkinsonism are _________, increased _____, and ________ instability

A

bradykinesia/akinesia, tone/rigidity, postural

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4
Q

Parkinsons’s is a chronic, progressive, neurodegenerative disease; get slow and selective loss of __________ dopaminergic neurons

A

substantia nigra

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5
Q

rest tremor, rigidity, bradykinesia, and postural instability, autonomic dysfunction, and neuropsychiatric disturbances are clinical features of what disease?

A

Parkinson’s

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6
Q

symmetry at ______, absence of ______ tremor, early dementia, _______ onset of symptoms, ______ disease progression, severe autonomic dysfunction, UMN or cerebellar signs, and early falling suggest a non-parkinson’s disease cause of parkinsonism

A
  • onset
  • rest tremor
  • abrupt
  • rapid
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7
Q
  • parkinsonian features
  • poor response to levodopa
  • early postural instability and speech difficulties
A

multiple system atrophy, striatonigral degeneration

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8
Q

multiple system atrophy with autonomic failure, parkinsonian features, pyramidal tract signs, cerebellar signs, and peripheral neuropathy

A

Shy Drager syndrome

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9
Q

postural tremor greater than resting tremor in __________ parkinsonism, reversible and treated with phenothiazines or metoclopramide

A

drug induced

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10
Q

ischemia to striatum, with history of HTN and strokes, MRI white matter changes

A

vascular parkinsonism

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11
Q

MPTP induced parkinsonism causes death of ________

A

substantia nigra neurons

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12
Q

most effective agent for treatment of Parkinson’s, used with carbidopa to block peripheral decarboxylase, crosses blood brain barrier and is converted to dopamine

A

levodopa

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13
Q

wearing off, dyskinesias caused by ________ of L-dopa and decreasing ability of ________ to store dopamine

A

short half life, nigral neurons

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14
Q
  • reduces motor fluctuations
  • reduces metabolism of dopamine
  • selegiline
A

MAO-B inhibitors

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15
Q
  • methyltransferase, named entacapone and tolcapone

- inhibit levodopa catabolism

A

COMT inhibitors

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16
Q
  • stimulate post synaptic dopamine receptors directly
  • effective for tremor, bradykinesia, rigidity
  • pramipexole, ropinirole, bromocriptine
  • stimulate mesolimbic system, bad side effects
A

dopamine agonists

17
Q
  • abnormal involuntary movements

- pathophysiology unknown, etiology unknown

A

hyperkinetic movement disorders

18
Q
  • rhythmic, predictable
  • essential most common
  • treat with primidone or propanolol
A

tremor

19
Q

arrhythmic and suppressible, urge to move, Tourette’s in childhood and adult onset, treat with neuroleptics that block dopamine

A

tics

20
Q
  • arrhythmic, insuppressible, sustained movements
  • writhing=athetosis
  • focal or generalized
  • due to lack of reciprocal inhibition
  • treat with Botox, anticholinergics, neuroleptics
A

dystonia

21
Q
  • non sustained, arrhythmic, ballistic movements
  • common diseases are hemi ballismus, huntington’s, post strep autoimmune
  • treat with dopamine blockers, anticholinergics (tardive)
A

chorea

22
Q
  • brief shock like movements
  • idiopathic, primary generalized epilepsies, post anoxic
  • treat w/ antiseizure meds, long acting benzodiazepines
A

myoclonus

23
Q
  • involuntary movements after use of dopamine blocking agents
  • treatment: increase dopamine blocker, anticholinergics to prevent
A

tardive dyskinesia