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38 Cards in this Set
- Front
- Back
Brachial Plexus
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C5-T1- upper limb
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Lumbosacral plexus
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L2-S4 lower limb
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Primary motor cortex
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precentral gyrus, area 4, M1, layer V pyramidal neurons
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Motor cortex type
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heterotypical agranular
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Area 6
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Premotor, supplementary motor
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Areas 5, 7
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parietal motor
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Areas 32, 24
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Cingulate motor
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Lower Motor Neurons
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synapse directly with skeletal muscles
anterior horn cranial n. motor neurons includes cell body and axon |
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Upper Motor Neurons
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synapse with other neurons, NOT muscles
corticospinal and corticonuclear tracts |
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Damage to lower motor neurons
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flaccid paralysis
hypotonia, hyporeflexia, atrophy, fasciculations |
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Damage to upper motor neruons
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spastic paralysis
hypertonia, hyperreflexia, no immediate atrophy (disuse atrophy appears later) |
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Brown-Sequard Syndrome
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Upper limb-- lower motor neuron signs
Lower limb- upper motor neurons signs |
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alpha motor neuron
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Large
flexors: posterior region of anterior horn extensors: anterior region of anterior horn |
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Gamma motor neuron
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small
flexors and extensors: distributed near alpha motor neurons |
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Lower motor neuron function:
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influenced by:
sensory feedback from muscles upper motor neurons that form the various descending tracts |
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Large motor unit
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600-1000 muscle fibers/lower motor neuron
for HIGH levels of force |
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small motor unit
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10-100 muscle fibers/lower motor neuron
for LOW levels of force, rapid contraction and fine control |
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size principle
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small motor units recruited first in muscle contraction
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motor unit
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motor neuron plus all the muscle fibers it innervates
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muscle spindles
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provide sensory input from muscles to lower motor neurons
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Static nuclear bag fiber
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mechanoreceptors respond to change in muscle length
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Dynamic nuclear bag fiber
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mechanoreceptors respond to RATE of change in muscle length
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Nuclear chain fiber
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mechanoreceptors respond to change in muscle length
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GTO
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mechanoreceptor that responds to change in muscle/tendon tension
type Ib-- inhibit alpha motor neurons to same muscle higher activation threshold |
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Alpha-Gamma coactivation
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voluntary movement-- activates alpha and gamma motor neurons simultaneously
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Spasticity
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increased resistance to passive movement
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Hypertonicity
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muscles exhibit increased tone but feel "weak" to patient
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Hyperreflexia
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deep tendon reflexes are more brush (0 to 4+ scale)
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Clonus
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repetitive oscillation between flexion and extension at a single joint due to hyperactive flexor and extensor reflexes
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Babinski sign
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great toe (inverted planar flexion) can be accompanied by "triple flexion"-- dorsiflexion at ankle, knee, hip
normal in children |
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Disuse atrophy
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develops slowly over a period of weeks to months to years
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corticonuclear signs of V
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typically no jaw deviation
deviation towards weak side |
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corticonuclear signs of VII
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contralateral, lower face sags
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corticonuclear signs of X
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uvula deviates to strong side
hoarse voice, swallowing difficulty |
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corticonuclear signs of XII
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tongue deviates to weak side
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corticonuclear signs of XI
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SCM, trapezius weak (I/L) side head cannot be turned C/L
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upper motor neuron lesion
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spasticity, hypertonia, hyperreflexia, clonus, babinski
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lower motor neuron lesion
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flaccidity, hypotonia, hyporeflexia, fasciculations, atrophy
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