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40 Cards in this Set
- Front
- Back
"movement disorder" |
basal ganglia |
|
UMN |
cortex, subcortex, brainstem, spinal cord |
|
LMN |
anterior horn cells, nerve roots, plexus, peripheral nerves |
|
duchennes |
x-recessive |
|
myotonic dystrophy |
autosomal dominant |
|
deletion/duplication at Xp21 |
duchennes |
|
CTG nucleotide repeat at chromosome 19 |
myotonic dystrophy |
|
prognosis of GBS |
stabilize after 3 weeks because schwann cells re-myelinate |
|
Tx GBS |
IVIG/plasmapharesis |
|
Dx GBS |
-EMG: conduction blocks* with slow velocity -high CSF protein (demyelination of nerve roots) |
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Schwann cells myelinate: |
PNS (GBS, charcot marie) |
|
oligodendrocytes myelinate: |
CNS (MS) |
|
where along the nerve are Na channels at the highest? |
-initial segment & node of Ranvier |
|
what type of reflex are muscle stretch reflexes? |
MONOSYNAPTIC (initiated by activation of muscle spindles) |
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pain at digits 1-3 and weak thumb, that AWAKENS PATIENT FROM SLEEP* |
median nerve entrapment at wrist |
|
weak hand, numb digits 4-5 |
Ulnar nerve entrapment at elbow |
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Saturday night palsy |
Radial entrapment at *SPIRAL GROOVE |
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Honeymooner's palsy |
Radial entrapment at *AXILLA |
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wrist drop |
radial nerve entrapment |
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wrist drop but TRICEPS OK, where is the radial nerve entrapment? |
At spiral groove* |
|
Pb toxicity |
radial nerve entrapment |
|
weak foot DORSIFLEXION (foot drop) & loss of sensation at 1st/2nd toes |
fibular nerve entrapment |
|
3 types of foot drop |
1. fibular nerve 2. L5 radiculopathy 3. ALS |
|
foot drop, pure weakness, sensation intact**** |
ALS |
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what are the muscles supplied by the fibular nerve? |
-tibialis ANTERIOR (foot dorsiflexion)//footdrop -peroneus longus (foot eversion) |
|
patient has paresthesias of lateral leg and dorsum of foot, has foot drop, and radiating back pain, what else can you expect with L5 radiculopathy? |
-poor hip abduction (gluteus medius) -poor knee flexion (hamstrings) -poor foot in*version (posterior tibialis) |
|
CMAP |
motor nerves |
|
SNAP |
sensory nerves |
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what results in reduced amplitude of CMAP? |
-AHC, root, plexus, axonal neuropathy
|
|
reduced snap |
-lesions DISTAL to DRG (plexus/periphearl nerve) |
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lesions PROXIMAL to DRG (radiculopathies) do what to SNAP? |
UNCHANGED |
|
conduction block*** on nerve studies |
GBS or carpal tunnel*** |
|
slowed conduction velocity*** |
demyelinating** polyneuropathy |
|
spontaneous discharge of INDIVIDUAL muscle fibers |
fibrillations (can only be seen in lab) |
|
spontaneous discharge of individual MOTOR UNITS |
fasciculations (can be seen VISUALLY by looking at the skin!!!) |
|
in what type of dz will you see LARGE AMPLITUDE MUPs on EMG? |
CHRONIC neurogenic conditions |
|
LARGE amplitude MUPs |
anything involving LMN (AHC, etc): adjacent*** previously denervated* muscle fibers are RE-INNERVATED....takes time to develop (so only seen in chronic conditions) |
|
when you increase the force of muscle contraction in CHRONIC neuro dz, recruitment* of additional motor units is DECREASED, why? |
fever numbers of motor units |
|
reduced amplitude of MUPs |
MYOPATHIES |
|
Why is there a random, scattered DROP out of individual muscle fibers from all motor units in myopathies? |
the muscle fibers in each motor unit are randomly lost, resulting in fewer muscle fibers per motor unit |