Lecture 8 Flashcards

(15 cards)

1
Q

what are the symptoms of a UMN lesion?

A
  • muscle weakness
  • hyper-reflexia
  • hypertonicity
  • positive babinski sign
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2
Q

what is the name for the combination of hyper-reflexia and hypertonicity?

A

spastic paralysis

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3
Q

why does hyper-reflexia occur with UMN injury?

A

if damaged, higher cortical areas cannot provide inhibitory or modular control to the reflexes

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4
Q

what are the two types of hypertonic symptoms?

A
  1. spasticity
  2. rigidity
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5
Q

what is the difference between spasticity and rigidity?

A

spasticity is rate and force dependant (more resistance as limb is moved faster), no change in rigidity with rate or force

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6
Q

what is the clasp-knife phenomenon?

A

when moving a spastic joint, it will resist right up until the end of the ROM

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7
Q

what is decorticate posture?

A

extreme flexor posturing

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8
Q

what is decerebrate posturing?

A

extreme extensor posturing

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9
Q

what does decorticate posturing indicate?

A

the lesion is above the midbrain and involves the rubrospinal tract

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10
Q

what does decerebrate posturing indicate?

A

the lesion is below the midbrain and involves the vestibulospinal tract

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11
Q

what is a positive Babinski sign?

A

toe extension

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12
Q

what is characteristic of a hemiplegic gait?

A

the hip is hiked up or circumducted to keep walking while the leg stays extended

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13
Q

what are the causes of upper motor neuron lesions?

A
  1. injury to the motor cortex
  2. damage to internal capsule/cerebral peduncles
  3. spinal cord lesion or compression
  4. diseases attacking upper motor neurons
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14
Q

describe primary lateral sclerosis

A
  • cause: unknown
  • mechanism: degeneration of UMNs
  • symptoms: UMN symptoms (i.e. spasticity, weakness)
  • treatment: no cure
  • speed: progresses slowly and non-fatal
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15
Q

describe amyotrophic lateral sclerosis

A
  • cause: unknown, some genetic component
  • mechanism: degeneration of UMNs and LMNs, glutamate build-up
  • symptoms: UMN and LMN symptoms
  • treatment: no cure, riluzole for glutamate
  • speed: progresses rapidly and often fatal 2-4 years later
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