dementias and movement disorders Flashcards

1
Q

Binswanger’s disease - type of dementia

A

Small vessel vascular dementia

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2
Q

Binswanger’s disease symptoms

A

4 Ds - Dementia, dysexecutive synd, delay (slow), depletion (apathy and amotivation)

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3
Q

Binswanger’s disease MRI

A

periventricular white matter abnormalities

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4
Q

Vascular dementia

4 Ds - Dementia, dysexecutive synd, delay (slow), depletion (apathy and amotivation)

A

Binswanger’s disease

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5
Q

Tauopathies

A

Alzheimer, FTD, CBD, PSP

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6
Q

alpha-synuclinopathies

A

Parkinson’s, MSA, lewy body dementia

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7
Q

Alzheimer’s pathology

A

Neuritic plaques, neurofibrillary tangles

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8
Q

Donepezil treats? Function? side effects

A

Alzheimer’s
cholinesterase inhib
insomnia, muscle cramp

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9
Q

Galantamine treats? Function? side effects

A

Alzheimer’s
cholinesterase inhib
wt loss, avoid with bad liver/kidney

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10
Q

Rivastigmine treats? Function, side effects

A

Alzheimers and Parkinson’s dementia
cholinesterase inhib
minimal - no liver mtab, no drug intxn

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11
Q

Memantine tx, function, side effects

A

Alzheimers
NMDA antagonist
Few side effects or interactions

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12
Q

Lewy body dementia sx

A

Fluctuating cognition
visual hallucinations
parkinsonism (after cognitive)

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13
Q

Parkinson’s disease DA agonists

A

Ropinirole
Pramipexole
Rotigotine
Apomorphine

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14
Q

Corticobasal degeneration sx

A
  • L-dopa unresponsive parkinsonism
  • alien hand
  • asymmetric limb dystonia, apraxia, myoclonus, neglect, cortical sensory loss
  • FT type dementia
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15
Q

Corticobasal degen imagine

A

asymmetric cortical atrophy

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16
Q

PSP sx

A
Axial rigidity
dysphagia
early falls
vertical (esp down) gaze palsy
FT type dementia
17
Q

PSP imaging

A

Midbrain atrophy (hummingbird sign)

18
Q

MSA sx

A

Parkinsonism and/or cbl dysfxn

severe autonomic dysfxn

19
Q

MSA imaging

A

“hot cross bun”

20
Q

Dopa-responsive dystonia sx

A
Twisted foot, gait abnormality
worse in evening
poss parkinsonism
child/young adult
very responsive low dose L-dopa
21
Q

Wilson’s disease gene & inheritance

A

Gene ATP7B copper transporter

AD

22
Q

Wilson’s disease dx

A

Dysarthria, gait change
tremor, dystonia, parkinsonism
psych disease, dementia

23
Q

Wilson’s disease imaging

A

T2 hyper, T1 hypo basal ganglia

24
Q

Wilson’s disease labs

A

24hr urine copper high, ceruloplasmin low

25
Q

Wilson’s disease treatments

A

Penicillamine
trientine
zinc

26
Q

Huntington’s gene

A

CAG trinuc repeat huntingtin gene, chr 4

27
Q

Huntington’s sx

A

Hyperkinetic mvt (chorea, myoclonus)
Poor voluntary mvt (dex, slurred speech)
Difficulty swallowing, falls

Subcortical cognitive - loss speed and flexibility

28
Q

Huntington’s tx

A

Tetrabenazine (only helps hyperkinetic mvts)

29
Q

Ataxia telangiectasia gene

A

ATM, chr 11. Immune!

30
Q

Ataxia telangiectasia sx

A

Ataxia
tiny red spidery veins (esp face), dilated vessels eyes
Frequent sinopulmonary infxns

31
Q

Ataxia telangiectasia labs

A

increased AFP, CEA

Decreased Ig G, A, E

32
Q

Neuroacanthocytosis sx

A

lip/tongue biting –> oral “eating’ dystonia, tics, chorea
akinetic/rigid feet
vertical ophthalmophegia
sz