Test 3 Neuro part 2 Flashcards

1
Q

decreased muscle tone
Passive movement without resistance
Nerve impulses lost
Flaccidity

A

Hypotonia

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2
Q

increased muscle tone
increased resistance to passive movement
Spasticity

A

hypertonia

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3
Q

What parts are involved with the lower motor neuron

A

Bulbar
Anterior horn cell
primary muscle
myoneural junction

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4
Q

what parts are involved with the upper motor neuron

A

Motor cortex
Internal capsule
Brainstem
spinal cord

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5
Q

what neurotransmitters are inhibitory

A

Dopamine and GABA

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6
Q

what neurotransmitters are excitatory

A

Acetylcholine

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7
Q

which motor neuron effects muscle groups, has minimal muscle atrophy, no fasciculations, increased DTR, hypertonia and spasticity, and has a babinski sign

A

Upper motor neuron (pyramidal)

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8
Q

which motor neuron effect individual muscles, has marked muscle atrophy, has fasciculations, decreased DTR, hypotonia and flaccidity, and does not have a babinski sign

A

lower motor neuron (antiriot horn and cranial nerve nuclei)

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9
Q

neurodegenerative disorderthat diffuselt affects upper and lower motor neuron of cerebral cortex, brain stem, and spinal cord
Selectively affects motor function
Progressive weakness leading to reparatory failure and death

A

Amyotrophic lateral sclerosis ALS

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10
Q

starts in the parental gyris

causes movement

A

pyramidal motor pathway

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11
Q

starts in the basil ganglia and modifies movement

A

extrapyramidal motor pathway

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12
Q

synthesizes and releases dopamine

A

substantia nigra

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13
Q

signal the corpus striatum to inhibit motor movement to make sure movement is controlled and smooth

A

dopamine

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14
Q

Voluntary movement paralysis, increased DTRs, babinski sign present, no involuntary movement, spastic muscle tone

A

pyramidal motor syndromes

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15
Q

little to no paralysis of voluntary movement, DTR slightly increased or WNL, absent babinski sign, tremor, chorea, athertosis, or dystonia, plastic or intermittent (cogwheel) rigidity

A

extrapyramidal syndromes

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16
Q

involuntary movements

A

dyskinesia

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17
Q

severe degernation/atrophy of basal ganglia (corpus striatum) involving dopaminergic pathwyas leading to impaired direct (movement facilitation) and indirect (movement inhibition) motor pathways
Defect of post synaptic receptors

A

Parkinsons Disease

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18
Q

movement that is slow, sinuous, distal extremities

19
Q

flapping hands

20
Q

reapid irregular contraction of muscle groups

21
Q

movement of face trunk and extremities

22
Q

traumatic injury of vertebral and neural tissues dut to compressing, pulling, or shearing forces
Loss of motor, sensory, reflex, and autonomic function below transected/ischemic area

A

spinal cord trauma

23
Q

Complete loss of reflex function at and below injury level; suprasegmental impulses inhibited
Paralysis, flaccidity, no sensation, no bladder or rectal control, hypothermia, hypotension
Over when reflexes return and spastic paralysis replaces flaccidity

A

spinal shock

24
Q

Loss of sympathetic outflow
Cervical/ upper thoracic injury
Unopposed parasympathetic (intact vagus nerve)
Vasodilation, hypotension, bradycardia, hypothermia

A

neurogenic shock

25
T1-L2 innervation
sympathetic nervous system
26
cranial nerve and sacral innervation
parasympathetic nervous system
27
sudden, massive, uncompensated CV response to SNS stimulation of sensory receptors below level of cord lesion
Autonomic hyperreflexia
28
plasma membrane disrupted, edema compresses capilares | Contralateral paresis, paralysis, dysphasia, dysphagia, agnosia
cerebrovascular accidents CVA
29
types of ischemic stroke
thrombotic | embolic
30
Arterial occlusions caused by thrombi formed in arteries supplying brain or in intracranial vessels transient ischemic attacks
Thrombotic stroke
31
fragments that break from throbs formed outside brain
embolic
32
location of CVA when there is bruit, retinal emboli, TIA history
Internal carotid
33
location of CVA when there is contralateral hemiparesis/plegia (UE>LE), contralateral sensory loss, aphasia/dysphasia, dysarthia, contralateral homonymous hemanopsia, hyperhidrosis, Cheyne-Stokes breathing
middle cerebral
34
location of CVA when there is contralateral hemiparesis/plegia/proprioception, tongue weakness/dysarthia
vertebral
35
location of CVA when there is contralateral hemiparesis (LE>UE), contralateral LE sensory loss, apraxia
anterior cerebral
36
location of CVA when there is contralateral hemiplegia and sensory loss, dyskinesia, ataxia, tremor, agnosia, bilateral: coma, visual loss, absent doll eyes and decrease LOC
posterior cerebral
37
Blood escapes from defective/injured vasculature into subarachnoid space and causes an inflammatory response Decreased LOC, positive Kernig and Brudzinski sign, photophobia, nuchal rigidity, papilledema
subarachnoid hemorrhage
38
inflammation and swelling of the optic nerve
papilledema
39
Progressive, inflammatory, demyelinating CNS disorder | Involves sensory and motor neurons
multiple sclerosis
40
Acquired inflammatory disease causing demyelination of peripheral nerves with relative sparing of axons Autoimmune disease preceded by viral or bacterial infection
Guillain-Barree syndrome
41
Chronic autoimmune disease IgG antibodies produced against acetylcholine receptors that act at neuromuscular junction Defect in nerve impulse transmission
Myasthenia Gravis
42
prolonged, uncontrollable sadness
Depression
43
Decreased neurotransmitter activity in major depression is caused by
Decreased receptro sensitivity Increased neurotransmitter release Increased neurotransmitter reuptake increased neurotransmitter metabolism by MAO
44
Excessive and persistent worries | Abnormalities in the norepinephrine and serotonin systems
GAD