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36 Cards in this Set

  • Front
  • Back
Define Motor Neuron disease, give examples
(Ant horn cell)
- disease within motor neurons cause secondary changes in motor axons and motor fibers
- ie. ALS, spinal muscular atrophy, polio, West-Nile
Define motor neuropathy, give examples
- disease that affects axons/myelin/both
- diabetes, renal insufficiency, lead
Define NMJ disease, give examples
- disease affecting pre or post synaptic areas of NMJ
- MG= post synaptic
- Eaton-Lambert- pre synaptic
Define Paresthesiae
- abnormal sensations (tingle, prick, pins, warm, cold, burn)
Define hyperesthesia
- loss of a larger sensory neurons that leads to the over activity in smaller axons
- mild stimuli = painful
Define Anesthesia
- no sensation 'numb'
What are teh 2 most common causes of autonomic symptoms?
1. diabetes
2. amyloid neuropathy (esp young patient)
What are some autonomic symptoms?
- dry skin, hair loss
- impotence, constipation/diarrhea, incontinence/urinary retention, postural hypotension
What is Gower's manuver?
- person has to climb up on themself in order to stand up
- hip weakness, weak thoracic muscles indicative of a myopathy
What is hypertrophy/ pseudohypertrophy of a muscle and give an example
- muscle bulk appears sufficient but is replaced by fat/connective tissue
- Duchenne muscular dystrophy in calves/deltoid
What are the 4 general categories of muscle weakness?
1. neuropathy
2. myopathy
3. motor neuron/ant horn
4. NMJ
Which category of weakness is mainly distal? proximal?
distal= neuropathy
proximal= myopathy
Which categories of weakness are usually decreased? normal?
Decreased= neuro/myo
Normal= ant horn/ NMJ
Which is the only category of weakness that shows sensory loss and paresthesias?
- neuropathy
Fasciculations are present in which category? possible in which category?
- present in Ant horn
- possible in neuropathy
Atrophy is present in all categories of weakness except?
- NMJ
Which category of weakness has severe fatigue?
- NMJ
Which is the category that never involves pain?
- NMJ
Nerve conduction study is evaluated by what 2 ways and what do they indicate?
1. amplitude (axonal damage)
2. velocity of response (demylination of nerve)
How does electromyography differentiate between neuropathy and myopathy?
N= not enough motor units firing to make a full view of the repeating unit
M= unit amplittude is smaller as it requires little stimulus to fire
What does CK levels indicate? How does this differentiate between neuropathy and myopathy?
- indicates muscle damage
N- normal CK
M= high CK
What is carpal tunnel classified under?
Compressive neuropathy (mononeuropathy)
Carpal tunnel usually involves what nerve?
Median
What is polyneuropathy characterize by?
- distal pain, paresthesia, weakness, neuro findings (ie motor impaired, hyporefleia)
What is the 2 most common cause of Acute polyneuropathy?
Guillain=Barre Syndrome (AIDP- ascending paralysis with weakness)
AIDS (severe and quick)
What is the ost common causeof subacute polyneuropathy?
Diabetic polyneuropathy
What is the most common cause(s) of chronic polyneuropathy and what is unique about this category?
- Charcot-Marie-Tooth
- HNPP
- Many of these are hereditary
Describe Guillian-Barrer's course and treatment
- 1/3 cases preceded by URI
- electrophysiological studies show demyelination
- Treat with IVIG (long)
What is a common NMJ disorder?
Myasthenia gravis
Describe the course, testing, treatment of Myasthenia gravis
- disease of post-synatpic NMJ, involves proximal and distal, curtain sign, fatiguable
- Tensilon test, electrodiagnositc
- Treat with steroids
What are the 2 most common inflammatory myopathies?
1. polymyositis
2. dermatomyositis
Describe dermatomyositis; signs, tests, those susceptible
- inflamed skin/muscle with minor clots at nail bed, rash on face
- muscular biopsy shows perifasicular atrophy
-females over 40
What would a muscle biopsy look like in an individual with polymyositis?
- wBC invasion into muscles
What is most often used to treat neuropathies?
- the anticonvulsant gabapentin
What are possible causes of the Ant Horn disease, ALS?
- sporadic (most and involves UMN/LMN)
- environment
- familial
What is the pathology and related clinical signs of ALS?
- CNS (brain and spine), dendrites atrophy, then axonal degeneration
- drool, foot drop, chocke, fingers weak, speech problems
- full cognition!