dementias and movement disorders Flashcards

(32 cards)

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
Wilson's disease treatments
Penicillamine trientine zinc
26
Huntington's gene
CAG trinuc repeat huntingtin gene, chr 4
27
Huntington's sx
Hyperkinetic mvt (chorea, myoclonus) Poor voluntary mvt (dex, slurred speech) Difficulty swallowing, falls Subcortical cognitive - loss speed and flexibility
28
Huntington's tx
Tetrabenazine (only helps hyperkinetic mvts)
29
Ataxia telangiectasia gene
ATM, chr 11. Immune!
30
Ataxia telangiectasia sx
Ataxia tiny red spidery veins (esp face), dilated vessels eyes Frequent sinopulmonary infxns
31
Ataxia telangiectasia labs
increased AFP, CEA | Decreased Ig G, A, E
32
Neuroacanthocytosis sx
lip/tongue biting --> oral "eating' dystonia, tics, chorea akinetic/rigid feet vertical ophthalmophegia sz