46,49,59,61 Flashcards

(38 cards)

1
Q

essential tremor affects which body parts

A

both hands and forearms and less commonly the head and voice

begins in one upper extremity and soon compromises the other.

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2
Q

age of onset in essential tremor

A

bimodal- 20s or 60s
unimodal- 50s

tremor frequency decreases with age

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3
Q

which drugs can exacerbate essential tremor

A

valproic acid

lithium

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4
Q

differential for essential tremor

A

Parkinson’s disease and dystonic tremor.

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5
Q

first line medical management for essential tremors depending on age

A

young- propranolol

old- primidone

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6
Q

surgical management for essential tremors

A

stereotactic thalamotomy and thalamic stimulation

target: ventralis intermedius nucleus of the thalamus.

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7
Q

posture. Involuntary sustained twisting is referred to as

A

dystonia

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8
Q

drugs that can cause dystonia

A

dopamine blocking drugs (neuroleptic/antipsychotics)

antiemetics (prochlorperazine or metoclopramide)

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9
Q

Focal dystonia commonly affects which muscles?

A

cervical muscles –> twisting of head to side (torticollis)

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10
Q

other types of focal dystonia

A

blepharospasm (an involuntary closure of the eyelids),

dystonic writer’s cramp,

spasmodic dysphonia,

oromandibular dystonia.

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11
Q

Young patients with focal dystonia should be

screened for

A

Wilson’s disease.

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12
Q

diagnosing focal dystonia

A

clinical

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13
Q

treatment for mild dystonia

A

nothing

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14
Q

treatment for severe dystonia

A

*botox- lasts up to 3-6 mo

anitcholinergics, benzos

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15
Q

type of gait in cerebellar dysfunction

A

wide based gait

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16
Q

cardinal features of cerebellar dysfunction

A

disturbances in motor control,
muscle tone regulation,
coordination of skilled movements.

17
Q

can speech be affected in cerebellar dysfunction?

A

yes- speech slurred- cerebellar dysarthria

18
Q

arterial supply of cerebellum and which main arteries they come from

A

PICA- vertebral artery

AICA- basilar

SCA- basilar

19
Q

The distal portions of PICA bifurcate into a medial trunk that supplies the _____ and a lateral trunk that supplies the ______

A

medial: vermis and the adjacent cerebellar hemisphere
lateral: cortical surface of the tonsil and cerebellar hemisphere.

20
Q

AICA supplies the

A

lateral tegmentum of the lower two-thirds of the pons

ventrolateral cerebellum.

21
Q

The _____ arises from AICA to supply the facial and auditory nerves.

A

internal auditory artery

22
Q

SCA supplies the .

A

superolateral cerebellar hemispheres,

superior cerebellar peduncle,

the dentate nucleus,

part of middle cerebellar peduncle

23
Q

cerebellar infarction (caused by thrombosis or embolus) presents with what?

A

severe vertigo, nausea, vomiting, and ataxia.

Loss of balance and difficulty maintaining posture, standing, and walking

24
Q

what can happen with bilateral or large cerebellar infarcts?

A

edematous cerebellum may compress the aqueduct of Sylvius or the fourth ventricle
–> obstructive hydrocephalus,

or may compress the brainstem–> decreased alertness.

25
With a cerebellar pressure cone, there is downward displacement of the cerebellar tonsils through the foramen magnum, resulting in
neck stiffness, cardiac and respiratory rhythm disturbances, apnea, and death.
26
With upward transtentorial herniation, there is upward displacement of the superior aspect of the cerebellar hemisphere through the edge of the _____ resulting in ____
tentorial incisura midbrain compression
27
Clinical manifestations of upward cerebellar herniation include
lethargy, coma, paralysis of upward gaze, midposition and unreactive pupils, and abnormal extensor posturing.
28
management of cerebellar infarcts
ICU, stroke unit ``` Emergency surgery (e.g., ventriculostomy or posterior fossa decompression or both) ```
29
most common dominantly inherited ataxia | in the world is ____
SCA 3 (Machado-Joseph disease)
30
SCA stands for
spinocerebellar ataxia
31
SCA 3 clinical features
progressive ataxia along with abnormalities of eye movements, speech, and swallowing. Onset-30s or 40s supranuclear ophthalmoparesis. Facial myokymia (resembling fasciculations)
32
SCA-1 presentation
begins with gait ataxia, and over time patients develop severe dysarthria and dysphagia. Ophthalmoparesis, spasticity, and choreoathetosis
33
most patients with SCA 1 become wheelchair bound within ___ years
15
34
SCA 6 presentation
milder, slow course mild sensory loss
35
SCA 7 is associated with
retinal degeneration.
36
SCA 10 is common in what population and has what manifestation
Mexican families seizures
37
SCA 12 is associated with
prominent early tremor of the arms and head
38
SCA 17 presentation (onset, features)
midlife cognitive decline and basal ganglia signs