VII- Neuron Dysfunction Flashcards

1
Q

UMN lesions paralyze

A

movements
-single possible movements

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2
Q

peripheral lesions paralyze

A

muscles
-so by destroying the nerve to the muscle the movements it does also deletes

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3
Q

hallmarks of UMN damage

A
  1. muscle weakness
  2. spastic paralysis/weakness
  3. inc muscle tone/hypertonia
  4. exaggerated reflex/hyperreflexia
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4
Q

clinical signs of UMN lesions

A
  1. clonus
  2. clasp knife effect
  3. pos babinski sign
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5
Q

hallmarks of LMN damage

A
  1. muscle weakness
  2. flaccid paralysis/weakness
  3. muscle wasting/atrophy
  4. hypotonia/dec tone
  5. reduced or absent reflexes
  6. fasciculations/spont muscle contractions
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6
Q

hallmarks of peripheral damage

A
  1. paralysis
  2. atrophy
  3. hypotonia
  4. fibrillations
  5. fasciculations
  6. areflexia

distinguish from LMN by sensory involvement and fibrillations

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7
Q

facial lesions

A

corticobulbar inputs bilaterally to upper half and contralat to lower
-UMN lesion contralat quarter lower face
-LMN lesion entire contralat half

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8
Q

extensor flexor imbalance

A

arms xs flexor tone + legs xs extensor tone = altered gait

UMN lesion

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9
Q

clonus

A

rapid, rhythmic contractions elicited by stretch of muscle
-over active stretch reflexes OR loss of inhibition from cortex = inc gamma neurons

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10
Q

clasped knife phenomenon

A

inc resistance to passive stretch of elbow extensors as moved into flexion > sudden collapse of resistance = easy flexion

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11
Q

hypertonicity/spasticity

A

inc resistance of flexors as extending esp with rapid attempts at passive movement
-from corticospinal tract disease

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12
Q

spinal muscular atrophy

A

SMN1 dysfunction = motor neuron death of LMNs
-weakness in upper legs, arms, trunk

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13
Q

myasthenia gravis

A

autoimmune so antibodies target acetylcholine receptors at NMJ
-weakness, rapid fatigue inc with exercise
-maybe respiratory failure, swallowing, breathing problems

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14
Q

ALS

A

both LMN and UMN so
-weakness, twitching, atrophy + stiffness, cramping

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15
Q

phases of spinal shock

A
  1. 0-1 days- areflexia/hyporeflexia, loss of descending nervous stim
  2. 1-3 days- initial return of reflexes from super sensitivity
  3. 1-4 weeks- hyperreflexia from new synaptic growth
  4. 1-12 months- hyperreflexia esp cutaneous from growth of long axons, mass reflex
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