CNS and PNS Flashcards

1
Q

UMN lesions (5)

A
  1. TBI
  2. CVA
  3. SCI
  4. MS
  5. Parkinson’s
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2
Q

Originates in anterior horn of SC and out into periphery. Skeletal mm. Cranial nerves. Efferent nerves

A

LMN

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3
Q

LMN lesions (4)

A
  1. Muscular dystrophy
  2. Polio
  3. Peripheral nerve injury
  4. Myasthenia gravis
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4
Q

Male genetic disorder. Proximal weakness first in pelvis then shoulder. Flexion contractures and scoliosis. Most severe

A

Duchenne Muscular Dystrophy DMD

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5
Q

Viral infection, induces flaccid weakness by damaging motor neurons. Don’t push too hard! Healing: motor units- mm hypertrophy- reinnervation

A

Post polio/poliomyelitis

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6
Q

Decreased comm b/t motor neuron and mm. Autoimmune common in females 20-30. Prox weakness (eyes, face) before distal (limbs)

A

Myasthenia Gravis

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7
Q

Temp paralysis and sensory loss. Peripheral nerve injury

A

Neuropraxia

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8
Q

Stretch or compression of axon. Peripheral nerve injury

A

Axonotmesis

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9
Q

Severed neuron. Peripheral nerve injury

A

Neuromesis

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10
Q

Neuromuscular disorders. (4)

A
  1. MS
  2. GBS
  3. ALS
  4. Parkinson’s
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11
Q

Chronic, slow progressing disease of CNS. Demylinated glial plaques of UMN. Etiology unknown

A

MS

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12
Q

Four types of MS

A
  1. Benign
  2. Exacerbating-Remitting
  3. Remitting-Progressive
  4. Progressive
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13
Q

MS w/ Abrupt onset. Almost complete remission. Little to no permanent functional disability

A

Benign MS

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14
Q

MS w/ sudden onset. Partial or complete remission. Remain stable for long periods of time

A

Exacerbating-Remitting MS

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15
Q

MS w/ gradual onset and potential for sudden symptoms in one area. Exacerbations expected. Progressive disability. Symptoms do not remit as completely.

A

Remitting-Progressive MS

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16
Q

MS w/ slow onset. Exacerbations. No remitting of symptoms resulting in severe disability. More common in men

A

Progressive

17
Q

MS symptoms (4)

A
  1. Motor function loss
  2. Fatigue
  3. Spasticity
  4. Incontinence
18
Q

Spasticity due to MS results from…

A

corticospinal demyelination

19
Q

MS. Slow, uncoordinated progression of reciprocal LE movements. Staggering, wide base gait, poor footing

20
Q

MS. Inability to perform rapidly alternating movements

A

Dysdiadochokinesia

21
Q

MS. Overreaching

22
Q

MS optic defects (3)

A
  1. Diplopia
  2. Optic neuritis
  3. Nystagmus
23
Q

MS speech (3)

A
  1. Slurring
  2. Dysphagia
  3. Dysarthria
24
Q

MS functional rehab (5)

A
  1. Bed mob
  2. Balance
  3. Amb
  4. Xfers
  5. Energy conservation
25
MS precautions (3)
1. Overstretching 2. Heat 3. Mm fatigue
26
Chronic progressive degenerative disease where rate of dopamine produced drops. Idiopathic onset.
Parkinson's
27
Parkinson's ACh>Dopamine=
Facilitation>inhibition
28
Parkinson's affects _______ which is outside the corticospinal tract
Extrapyramidal (EP) system
29
EP system regulates (3)
1. Posture 2. Righting reactions 3. Initiate movement
30
Parkinson's s/s (4)
1. Tremors 2. Rigidity 3. Postural reflex loss 4. Bradykinesia
31
Parkinson's rehab
controlled mobility w/ rotation
32
Both UMN and LMN. Degeneration of motor cells in frontal cortex, parietal lobe, cranial nerve nuclei, and anterior horn. Male more common
ALS
33
Two tracts most affected by ALS
Corticospinal and corticobulbar
34
ALS symptoms occur ______ first
Distally
35
ALS rehab focus (5)
1. ADs 2. Low rep 3. Xfer 4. Deep breathing 5. Shoulder mobs
36
Acute, demyelination of cranial and spinal nerves. Re-myelination typically occurs. Attacks spinal and cranial roots
GBS
37
GBS s/s (2)
1. Symmetrical distal-prox weakness | 2. Proprioceptive loss> sensory
38
GBS acute rehab (2)
1. Respiration | 2. Maintain ROM
39
GBS subacute rehab
PNF Iso-ecc-conc