Movement/Tic D/Os Flashcards

1
Q

Parkinson’s disease treated with levodopa develops VHs. Recommendations?

A

Reduce dose of levodopa

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2
Q

What MRI finding would most specifically indicate a diagnosis of Huntington’s disease?

A

Caudate head atrophy

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3
Q

65 y/o with h/o asthma presents tx of essential tremor.

First line tx?

A

Primidone

Avoid beta blockers

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4
Q

42 y/o M with gradually progressive cognitive deficits also develops jerking movements of extremities, head, and trunk.
MRI - atrophy caudate nuclei BL.
Pts father had similar issues that started at 50.
Which test is most likely to confirm dx?

A

DNA analysis for CAG repeats

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5
Q

79 y/o pt with decreasing mental state over 3 weeks has an exaggerated startle response with violent myoclonus (elicited by turning on room lights, speaking loudly, or touching the patient).
Myoclonic jerks occur spontaneously. Ataxia.
EEG - sharp waves.
Dx?

A

Subacute spongiform encephalopathy

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6
Q

Med useful in management of orthostatic hypotension in Parkinson’s?

A

Fludrocortisone

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7
Q

Tx of Huntington’s chorea

A

Haldol

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8
Q

98 y/o M in ER. Unconscious after choking. Had progressive neuro condition presented in early 30’s with involuntary, irregular movements of all extremities and face. After 15 yr course evolved into rigid, akinetic condition with difficulty swallowing and speaking. Progressive dementia and full time care. Postmortem exam showed generalized brain atrophy.
Dx?

A

Huntington’s

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9
Q

Gait consisting of: postural instability, festination (shortening strides and moving feet more quickly to accelerate),and truncal rigidity.
Lewy bodies visualized.
Involuntary acceleration is seen in what condition?

A

Parkinson’s

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10
Q

35 y/o with history of 2 year cognitive deterioration, difficulty at work, and irritability.
Restless with slow, writhing movements in most muscle groups and frequent blinking.
Father and grandpa had similar sxs and died in their 50s.
Dx?

A

Huntington’s

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11
Q

Pt with depression. 3 yr hx of change in personality. Irritability. Impulsive outbursts. Eccentric or inappropriate social interactions. Lost job. Now withdrawn and fidgety.
Increased eye blinking, marked tongue impersistence, mild bradykinesia, akinesia, and mild hyperreflexia w/o clonus.
Pts dad died of severe dementia at 55.
Dx?

A

Huntington’s

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12
Q

Typical of idiopathic Parkinson’s disease, rather than another Parkinsonian syndrome

A

Aysmmetrical onset and progression of motor symptoms

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13
Q

First line tx for restless legs

A

Pramipexole

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14
Q

Multifocal myoclonus in comatose pt indicates

A

Metabolic encephalopathy

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15
Q

Most effective tx for writer’s cramp (focal dystonia associated with writing)?

A

Botulinium toxin

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16
Q

Essential tremor improves with

A

reaching for objects (action)

17
Q

Most prevalent mvmt d/o in those > 70 y/o?

A

Essential tremor

18
Q

6 y/o with 4 wks of intense eye-blinking and lip pursing that waxes and wanes, increases
with stress.
Family Hx of tic d/o.
First step?

A

Explain to family that it may be transient

19
Q

Diagnosis w/ trinucleotide repeat expansion

A

Huntingtons

20
Q

Treatment for Huntington’s Disease

A

High potency Antipsychotics

21
Q

25 yo pt w/ several year cognitive decline, dysarthria, dysphagia, and slow mvmts. Has hand tremor which increases in amplitude on arm extension. Also has hepatic disease of unknown etiology. Ocular exam reveals golden brown ring around cornea. Can confirm dx w/ blood
test for?

A

Ceruloplasmin

22
Q

For which pt would ordering a serum ceruloplasmin be indicated?

A

Young adult M w/ new onset emotional lability and mvmt d/o

23
Q

Huntington’s disease etiology classified as polymorphism d/t what property?

A

Region has many alleles differing in # of CAG repeats