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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)

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)

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

Saturday night palsy

Radial entrapment at *SPIRAL GROOVE

Honeymooner's palsy

Radial entrapment at *AXILLA

wrist drop

radial nerve entrapment

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

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

what results in reduced amplitude of CMAP?

-AHC, root, plexus, axonal neuropathy


reduced snap

-lesions DISTAL to DRG (plexus/periphearl nerve)

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