Ch 6 Neurologic Exam Part II Flashcards

(49 cards)

1
Q

Define akinesia

A

lack of movement

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2
Q

Define athetosis

A

slow, continuous, involuntary writhing movement that prevents maintenance of a stable posture

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3
Q

Define chorea

A

irregularly timed excessive jerky movements

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4
Q

Define ballismus

A

extreme choreiform movement

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5
Q

What are tone abnormalities

A

resistance to passive stretching of a joint.

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6
Q

What are upper motor neurons? (UMN)

A

They include projections from the cortex to spinal cord (corticospinal tract) including the part that crosses in the medulla (pyramidal tract)

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7
Q

What are lower motor neurons? (LMN)

A

They include projections from the brainstem and spinal cord, via motor nerves to innervate skeletal muscle

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8
Q

Hyperreflexia and increased tone are indicative of what type of lesions

A

Upper motor neuron lesions (UMN)

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9
Q

atrophy, fasiculations, hyporeflexia can be indicative of what type of lesions?

A

Lower motor neuron lesions (LMN)

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10
Q

Pronator drift reflects problems in which area?

A

Upper motor neurons

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11
Q

Stereognosis

A

the ability to perceive and recognize the form of an object in the absence of visual and auditory information

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12
Q

graphesthesia

A

the ability to recognize writing on the skin purely by the sensation of touch

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13
Q

Gait abnormalities can be described in which 5 ways?

A
spastic
scissored
steppage
parkinsonian
ataxic
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14
Q

Spastic gait

A

spastic hemiparesis

when affected leg swings in arc motion

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15
Q

Scissored gait

A

corticospinal dysfunction

gait appears stiff and thigh crosses over in front of the other thigh

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16
Q

steppage gait

A

when a foot or both feet are weak, resulting in foot drop

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17
Q

parkinsonian gait

A

short shuffling steps
person has difficulty starting or stopping
stooped over, arm swing reduced

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18
Q

ataxic gait

A

unsteady, wide based gait
hard to turn
cerebellar dysfunction

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19
Q

What is dysmetria? Where is the dysfunction located in the brain?

A

touching nose and examiner’s finger

ipsilateral cerebellar hemispheric dysfunction

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20
Q

What is dysdiadocholinesia?

Where is the dysfunction located in the brain?

A

switching hand movements facing up to palm facing down

ipsilateral cerebellar hemispheric dysfunction

21
Q

heel shin test assesses what

A

cerebellar functions in lower extremity

22
Q

Romberg test

A

stand with feet together, eyes closed

23
Q

romberg sign

A

unsteadiness within several seconds of closing eyes
suggests poor proprioception
dysfunction in posterior column of spinal cord
Vitamin b12 deficiency

24
Q

What do deep tendon reflexes evaluate?

A

evaluate afferent and efferent functioning

25
How is DTR assessed
single brisk tap from reflex hammer on skin of tendon
26
DTR increased reflexes (hyperactive)
corticospinal dysfunction
27
DTR decreased reflexes (hypoactive)
peripheral nerves or nerve roots dysfunction
28
dysfunction of corticospinal tracts can lead to what? seen in what condition
``` ipsilateral paralysis (inability to move) paresis (decreased motor strength) hypertonia (increased tone) long tract signs seen in normal pressure hydrocephalus ```
29
long tract signs mean?
symptoms that are attributable to the involvement of the long fiber tracts in the spinal cord. signs related to UMN lesions
30
example of long tract signs
e.g. spasticity, hyperreflexia, and abnormal reflexes such as Babinski or Hoffman's sign
31
Babinski sign can indicate what condition
corticospinal system dysfunction | UMN dysfunction
32
Define blown pupil
pupil that is dilated and unresponsive to changes in light
33
What is Babinski sign
fanning of toes and upward flexion of big toe (extensor plantar response)
34
Define bilateral temporal hemianopsia
loss of visual temporal fields due to a abnormality in optic chiasm
35
Clonus
repetitive, involuntary vibratory movement
36
Diplopia
experience of double vision
37
hemianopsia
loss of visual hemifield
38
homonymous
on the same side
39
Lower motor neuron
Motor neuron that originate in the anterior horn of spinal cord / brainstem and project to skeletal muscles
40
Nystagmus
rapid involuntary eye movement | can be lateral, vertical, rotational or mixed
41
Proprioception
perception of one's body position in space (based on sensory input from muscles and tendons)
42
Quandrantopsia
loss of one quadrant of visual field
43
Spasticity
increased muscle tone or increased resistance to stretching
44
Upper motor neuron
neurons that originate from the cerebral primary motor cortex (precentral gyrus) or from certain brainstem nuclei
45
Vestibular
sense of balance
46
Pyramidal Tract
- divides into corticospinal and corticobulbar tract - part of the UMN system - system of efferent nerve fibers - originate in the cerebral cortex and carry signals from the cerebral cortex to brainstem or spinal cord - responsible for voluntary control of body and face muscle
47
Corticobulbar tract
motor cortex to cranial nerve | controls voluntary movement of the muscles of the face, head and neck
48
Extrapyramidal tract
- originate in the brain stem - carrying motor fibers to the spinal cord - responsible for the involuntary and automatic control of muscle tone, balance, posture and locomotion
49
Corticospinal tract
motor cortex to LMN in spinal cord | controls voluntary movement of the muscles of the limbs and trunk