Anatomy and Physiology XVI Flashcards

1
Q

Where is the second synapse in the spinothalamic tract pathway?

A

VPL of the thalamus (p.428)

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2
Q

Where is the second synapse in the lateral corticospinal tract pathway?

A

Neuromuscularjunction (p.428)

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3
Q

Describe the location and path of the third order neuron in the DCML spinal pathway.

A

Sensory cortex (p.428)

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4
Q

Describe the location and path of the second order neuron in the spinothalamic tract pathway.

A

Sensory cortex (p.428)

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5
Q

Compare and contrast UMN lesions to LMN lesions with regards to weakness.

A

Weakness is present in both UMN and LMN lesions (p.428)

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6
Q

Compare and contrast UMN lesions to LMN lesions with regards to atrophy.

A

No atrophy in UMN lesions; atrophy in LMN lesions (p.428)

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7
Q

Compare and contrast UMN lesions to LMN lesions with regards to fasciculations.

A

No fasciculations in UMN lesions but present in LMN lesions (p.428)

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8
Q

Compare and contrast UMN lesions to LMN lesions with regards to reflexes.

A

Hyperreflexive in UMN lesions; hyporeflexive in LMN lesions (p.428)

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9
Q

Compare and contrast UMN lesions to LMN lesions with regards to tone.

A

Increased tone in UMN lesions; decreased tone in LMN lesions (p.428)

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10
Q

Compare and contrast UMN lesions to LMN lesions with regards to Babinski.

A

Positive babinski in UMN lesions; negative babinski in LMN lesions (p.428)

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11
Q

Compare and contrast UMN lesions to LMN lesions with regards to spastic paralysis.

A

Present in UMN lesions, not present in LMN lesions (p.428)

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12
Q

Compare and contrast UMN lesions to LMN lesions with regards to flaccid paralysis.

A

Absent in UMN lesions, present in LMN lesions (p.428)

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13
Q

Compare and contrast UMN lesions to LMN lesions with regards to clasp knife spasticity.

A

Present in UMN lesions, not present in LMN lesions (p.428)

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14
Q

Describe three clinical characteristics associated with LMN lesions.

A

Everything ‘lowered’ –> less muscle mass, decreased muscle tone, decreased reflexes, downgoing toes (p.428)

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15
Q

Describe three clinical characteristics associated with UMN lesions.

A

Everything ‘up’ –> increased tone, increased DTRs, upward pointing toes (p.428)

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16
Q

In what conditions are the anterior horns of the spinal cord exclusively affected?

A

Poliomyelitis and Werdnig-Hoffman disease (p.429)

17
Q

What characteristics are associated with spinal cord lesions to the anterior horns?

A

LMN lesions only with flaccid paralysis (p.429)

18
Q

What areas of the spinal tract are destroyed in MS?

A

Random and asymmetric lesions, mostly in the white matter of the cervical region (p.429)

19
Q

What causes lesions of the spinal tract in MS?

A

Demyelination (p.429)

20
Q

Name three characteristics of spinal cord lesions associated with MS.

A

Scanning speech, intention tremor, nystagmus (p.429)

21
Q

What areas of the spinal cord are lesioned in ALS?

A

Anterior horns and lateral corticospinal tracts (p.429)

22
Q

What sorts of deficits are seen in patients with ALS?

A

Combined UMN and LMN deficits with no sensory, cognitive, or oculomotor deficits; both UMN and LMN signs are present (p.429)

23
Q

What genetic defect can be associated with ALS?

A

Superoxide dismutase 1 defect (p.429)

24
Q

How does ALS commonly present?

A

Fasciculations with eventual atrophy; progressive and fatal (p.429)

25
Q

What treatment has been modestly shown to increase survival in ALS patients?

A

Riluzole treatment (p.429)