Neuromuscular Disease in Small Animals Flashcards

1
Q

what is the motor unit?

A

cell body in spinal cord
nerve root
spinal nerve
specific named nerve
synapse/junction
muscle fibers

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2
Q

what does it mean that myelinated nerves have saltatory conduction?

A

jump from one node of ranvier to the next

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3
Q

what is the rate of action potential travel influenced by?

A

diameter of axon and degree of myelination

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4
Q

how do the amount of acetylcholine receptors compare to the amount needed to generate an end-plate potential?

A

many more than required to reach action potential in the myofiber

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5
Q

how aree myofibers innervated?

A

each one innervated by only on axon of one motor neuron

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6
Q

what are some diseases that have an acute presentation?

A

myasthenia gravis
idiopathic polyradiculoneuritis

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7
Q

what is important about signalment?

A

breed
specific age groups

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8
Q

what are gait and posture like with neuromuscular disease?

A

lower motor neuron paresis without ataxia
crouched or plantigrade stance
cervical ventroflexion in cats
maybe worsens with exercise

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9
Q

should proprioception be normal or abnormal with neuromuscular disease?

A

normal with weight support

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10
Q

what are the goals of a workup for neuromuscular disease?

A

confirm neuromuscular localization
find level of lesion
define cause of lesion
determine treatment plan

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11
Q

what is important on a chem for diagnostics?

A

CK/AST

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12
Q

what does electrodiagnostic testing have a high degree of sensitivity for?

A

axonal dysfunction

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13
Q

what does electromyography record and study?

A

insertional, spontaneous and voluntary electrical activity of muscle

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14
Q

what can electromyography give insights into?

A

myopathies and neuropathies

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15
Q

what are abnormal electromyography findings?

A

spontaneous activity seen with no movement of the needle

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16
Q

what is evaluated for motor nerve conduction velocity?

A

CMAP amplitude: health of axons
nerve conduction velocity: degree of myelination

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17
Q

what are F waves?

A

antidromic motor nerve activation

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18
Q

what are diagnostics useful for in neuromuscular disease?

A

differentiate between denervation atrophy (axonal disease) and disuse atrophy

19
Q

what is the other name of idiopathic polyradiculoneuritis?

A

coonhound paralysis

20
Q

how can you diagnose idiopathic polyradiculoneuritis?

A

absent F waves

21
Q

which nerves are affected first by geriatric onset laryngeal paralysis polyneuropathy?

A

longest ones: sciatic nerve and recurrent laryngeal nerve

22
Q

what is the focal form or myasthenia gravis?

A

megaesophagus

23
Q

what is the generalized form of myasthenia gravis?

A

megaesophagus
appendicular muscle weakness, exercise intolerance
normal spinal reflexes and muscle tone

24
Q

what does acetylcholinesterase do?

A

enzymatic hydrolysis of unbound acetylcholine: rapid termination to ready muscle for next signal

25
Q

what is the end-plate potential like at a normal neuromuscular junction?

A

several times larger than that required to reach action potential in the myofiber

26
Q

what does the strength of muscle contraction depend on?

A

number of motor units activated in a muscle

27
Q

what are some nerve changes due to damage?

A

demyelination
axonopathy
axonopath with secondary demyelination
wallerian degeneration

28
Q

what is a polyneuropathy with acute presentation?

A

idiopathic polyradiculoneuritis

29
Q

where in the neuromuscular junction is the problem in myasthenia gravis?

A

postsynaptic membrane

30
Q

what does finding an elevated temperature, increased respiratory rate and/or effort, reduced chest excursions, or a palpable mass raise concern for?

A

aspiration pneumonia
hypoventilation
megaesophagus

31
Q

what findings on physical exam would suggest cranial nerve deficits?

A

fatiguing or absent palpebral reflex
dysphagia
megaesophagus
voice change
inspiratory noise/stridor

32
Q

what diagnostics for electrodiagnostic testing are useful for neuromuscular disease?

A

EMG
nerve conduction

33
Q

what are myotonic discharges on EMG like?

A

waxing and waning

34
Q

what is the most common cause of myotonic discharges on EMG?

A

myotonia congenita

35
Q

what is motor nerve conduction velocity used in conjunction with?

A

EMG to differentiate neuropathies from myopathies

36
Q

what does CMAP amplitude in motor nerve conduction velocity reflect?

A

health of the axons

37
Q

what is repetitive nerve stimulation used to evaluate?

A

neuromuscular junction

38
Q

what in repetitive nerve stimulation suggests myasthenia gravis?

A

decrement of greater than 10% of CMAP

39
Q

what are the clinical signs of idiopathic polyradiculoneuritis?

A

reduced or absent spinal reflexes
reduced muscle tone

40
Q

who does geriatric onset laryngeal paralysis polyneuropathy usually occur in?

A

geriatric (8-13) large breed dogs

41
Q

what is the result of geriatric onset laryngal paralysis polyneuropathy?

A

distal axonopathy with secondary demyelination

42
Q

what are the late clinical signs of geriatric onset laryngeal paralysis polyneuropathy?

A

laryngeal weakness or paralysis
paraparesis
abnormal withdrawal reflex

43
Q

what are the acquired forms of myasthenia gravis?

A

idiopathic
paraneoplastic: thymoma

44
Q

what is the acute, fulminating form of myasthenia gravis?

A

megaesophagus
appendicular muscle weakness, exercise intolerance
decreased or absent spinal reflexes, decreased muscle tone
hypoventilation, respiratory failure