Movement CPC Flashcards

1
Q

Understand the neuro exam of coord and gait

A

1) mental status
2) reflexes
3) sensory
4) Cranial nerves
5) coordination

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2
Q
Testing aspects of coordination 
- Rapid speech
lalalalala
pappapa
cacacaca
A

CN 12
CN 7
CN 10

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3
Q

different ways to examine tremor

A

while at rest
holding arms up against gravity
touch finger to nose and extend all the way

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4
Q

how to test rapid alternating movements

A

flip hands over and over

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5
Q

how to test precision hand movements

A

tap index and thumb then diff fingers

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6
Q

how to test drift
if pronator drift, means…

if drifts out then ….

A

close eyes and pretend holding pizza box in front of you

pronator drift = pyramidal tract dysfunction
if drift out = cerebellar dysfunction

make head move side to side for subtle drift

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7
Q

different movement tests

A

heel shin –> toes

foot rapid alternating movements (tap toes on examiner hands and toe to examiner finger)

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8
Q

check reflexes

A

make fist
push against resistance
then remove to see antagonist

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9
Q

how to check rebound

how to check romberg

how to check pull test

A

rebound = elevate, you pull down, leg go and see arms bounce up

romberg = close eyes and arm by side to see if arms swaying
(cerebellar problem)

pull = pull patient back and see how many step back they make

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10
Q

different kinds of gait

A

1) tandem
2) forced = walk on toes, heel, outside feet
3) casual = length, posture, tempo

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11
Q

how to check different gaits

1) neuropathic
2) hemiplegic
3) diplegic
4) L5 radiculopathy
5) choreiform gait
6) waddling/trendelenberg

A

1) neuropathic = periph nerve disease, high gait
2) hemiplegic = UMN lesion on one side , arm tuck, spasticity
3) diplegic = LMN&raquo_space; UMN problem, swinging gait on both sides, adducted kenes
4) L5 radiculopathy = neuropathy
5) choreiform gait = foot drop and step
6) waddling/trendelenberg

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12
Q

Features of dementing disease

A

1) impaired language
2) impaired long term memory
3) impaired planning, behavior, judgment
4) impaired short term memories

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13
Q

features of movement disorder
basal ganglia

vs cerebellar

A

basal ganglia
= resting tremor,
= hypokinesis = bradykinesis and rigidity
= hyperkineiss = chorea, athetosis, akathesia

cerebellum
= HANDS tremor

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14
Q

how is PSP and Alzheimer’s similar and diff

A

both tauopathies
PSP = movement
alzheimer = dementing

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15
Q

how is parkinson’s similar and diff from lewy body

A

both synucleinopathies
parkinson’s = movement
diffuse lewy body = demeting

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16
Q

recognize that various disease processes affect specific neuroanatomic site manifest similarly

A
substantia nigra
affected in 
1) parkinson's
2) multiple system atrophy
3) PSP
4) corticobasal degeneration

all present with parkinsonian like symptoms

17
Q

Key histologic hallmarks of the “synucleinopathies”:

1. Parkinson disease

A

1) lewy bodies
2) lewy neuritis (protein around neurons)
3) subst nigra degeneration with few neurons + gliosis

18
Q

Key histologic hallmarks of the “synucleinopathies”:

  1. Multiple System Atrophy
A

1) glial cytoplasmic inclusions
2) axonal and neuronal inclusions
3) gliosis and glial scars
4) diffuse degeneration of brainstem, putamen

19
Q

extrapyramidal signs

basal ganglia vs cerebellar disorders

A

a