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38 Cards in this Set

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

normal in children
Disuse atrophy
develops slowly over a period of weeks to months to years
corticonuclear signs of V
typically no jaw deviation
deviation towards weak side
corticonuclear signs of VII
contralateral, lower face sags
corticonuclear signs of X
uvula deviates to strong side
hoarse voice, swallowing difficulty
corticonuclear signs of XII
tongue deviates to weak side
corticonuclear signs of XI
SCM, trapezius weak (I/L) side head cannot be turned C/L
upper motor neuron lesion
spasticity, hypertonia, hyperreflexia, clonus, babinski
lower motor neuron lesion
flaccidity, hypotonia, hyporeflexia, fasciculations, atrophy