Neurologic Causes of Weakness and Paralysis Flashcards

1
Q

a reduction in the power exerted by muscle

A

weakness

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2
Q

inability to sustain performance of an activity that should be normal for a person of same age, sex, and size

A

fatigability

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3
Q

prevents adequate feedback information

A

proprioceptive sensory loss

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4
Q

increased time for full power to be exerted

A

bradykinesia

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5
Q

disorder of planning and initiating a skilled/learned mov’t

A

apraxia

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6
Q

weakness so severe that muscle can’t be contracted at all

A

paralysis

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7
Q

less severe weakness

A

paresis

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8
Q

refers to one half of body

A

“hemi-“

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9
Q

both legs

A

“para-“

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10
Q

four limbs

A

“quadri-“

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11
Q

myopathic weakness is marked in

A

proximal muscles

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12
Q

no specific pattern

A

neuromuscular junction weakness

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13
Q

resistance of a muscle to passive stretch

A

tone

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14
Q

increase in tone associated with disease of UMN

A

spasticity

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15
Q

velocity-dependent, sudden release after reaching maximum “clasp-knife”

A

spasticity

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16
Q

hypertonia that is present throughout the range of motion
lead-pipe or plastic stiffness
affects flexors and extensors equally

A

rigidity

17
Q

has a cogwheel quality that is enhanced by voluntary mov’t of contralateral limb
seen in extrapyramidal symptoms

A

rigidity

18
Q

increased tone that varies irregularly; from disease of frontal lobes

A

paratonia or gegenhalten

19
Q

decreased tone

A

flaccidity

20
Q

weakness with decreased tone or normal tone occurs with disorders of what

A

motor units

21
Q

refers to a single lower motor neuron and all the muscle fibers it innervates

A

motor unit

22
Q

muscle bulk is generally not affected by

A

UMN lesions

23
Q

atrophy is conspicuous in what lesion

A

LMN lesions

24
Q

muscle stretch reflexes are increased when?

A

UMN

25
Q

hyperreflexia in UMN lesions is usually accompanied by

A

loss of cutaneous reflexees

26
Q

tendon reflexes are ____ in myopathic weakness except in advances stages

A

preserved

27
Q

in this neuromuscular junction disorder, reflex responses are enhanced by previous voluntary activity (low to high)

A

Lambert-Eaton myasthenic syndrome

28
Q

in this neuromuscular junction disorder, reflex responses are depressed by previous voluntary activity (high to low)

A

myasthenia gravis

29
Q

neuropathic (LMN) vs myopathic

distal weakness

A

neuropathic (LMN)

30
Q

neuropathic (LMN) vs myopathic

symmetric proximal weakness

A

myopathic

31
Q

visible or palpable twitch and early atrophy indicates what lesion

A

neuropathic (LMN)

32
Q

hemiparesis

A

brain CT or MRI

33
Q

paraparesis

A

UMN - cerebral signs?
yes, CT scan (if none, spinal MRI)
no, spinal MRI (if none, myelogram/brain MRI)

LMN - EMG and NCS

34
Q

quadriparesis

A
if alert, UMN (spinal MRI) 
or LMN (EMG and NCS)

if not, CT scan or MRI

35
Q

monoparesis

A

UMN (brain CT or MRI)

LMN (EMG and NCS)

36
Q

distal, proximal, rectricted weakness

A

EMG and NCS

37
Q

electromyography (EMG) and nerve conduction studies (NCS)

A

UMN pattern -> spinal MRI
LMN pattern -> anterior horn, root, or peripheral nerve disease
myopathic -> muscle or neuromuscular disease