46,49,59,61 Flashcards

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
Q

With a cerebellar pressure cone, there is downward displacement of the cerebellar tonsils through the foramen magnum, resulting in

A

neck stiffness, cardiac and respiratory rhythm disturbances, apnea, and death.

26
Q

With upward transtentorial herniation, there is upward displacement of the superior aspect of the cerebellar
hemisphere through the edge of the _____ resulting in ____

A

tentorial incisura

midbrain compression

27
Q

Clinical manifestations of upward cerebellar herniation include

A

lethargy, coma, paralysis of upward gaze, midposition and unreactive pupils, and abnormal extensor posturing.

28
Q

management of cerebellar infarcts

A

ICU, stroke unit

Emergency surgery (e.g., ventriculostomy or
posterior fossa decompression or both)
29
Q

most common dominantly inherited ataxia

in the world is ____

A

SCA 3 (Machado-Joseph disease)

30
Q

SCA stands for

A

spinocerebellar ataxia

31
Q

SCA 3 clinical features

A

progressive ataxia along with abnormalities of eye
movements, speech, and swallowing.

Onset-30s or 40s

supranuclear ophthalmoparesis.

Facial myokymia (resembling fasciculations)

32
Q

SCA-1 presentation

A

begins with gait ataxia, and over time patients develop severe dysarthria and dysphagia.

Ophthalmoparesis, spasticity, and choreoathetosis

33
Q

most patients with SCA 1 become wheelchair bound within ___ years

A

15

34
Q

SCA 6 presentation

A

milder, slow course

mild sensory loss

35
Q

SCA 7 is associated with

A

retinal degeneration.

36
Q

SCA 10 is common in what population and has what manifestation

A

Mexican families

seizures

37
Q

SCA 12 is associated with

A

prominent early tremor of the arms and head

38
Q

SCA 17 presentation (onset, features)

A

midlife

cognitive decline and basal ganglia signs