L26 - muscle weakness Flashcards

1
Q

UMN origin

A

primary motor cortex

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2
Q

LMN origin

A

ventral horn of spinal cord

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3
Q

how to examine weakness

A

look for positive signs such as muscle volume, strength, tone, reflexes and involuntary movements
(observation, sensory, tone, power, reflexes)

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4
Q

muscle tone of UMN causes of muscle weakness

A

increased

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5
Q

reflexes in UMN causes of muscle weakness

A

increased

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6
Q

plantars in UMN muscle weakness

A

increased

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7
Q

muscle tone of LMN causes of muscle weakness

A

decreased

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8
Q

reflexes in LMN causes of muscle weakness

A

decreased

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9
Q

plantars in LMN muscle weakness

A

decreased

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10
Q

causes of UMN muscle weakness

A

stroke
infection
tumour
degeneration

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11
Q

clinical findings in UMN muscle weakness

A

weakness
mild atrophy
brisk reflexes
upping plantars

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12
Q

clinical findings in LMN muscle weakness

A

weakness
mild atrophy
depressed or absent reflexes
down going plantars

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13
Q

common LMN pathologies in muscle weakness

A
muscle
neuromuscular junction
nerve
root pathology
anterior horn
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14
Q

natures of LMN muscle weakness

A
  • axonal loss pathology

- demyelination pathology

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15
Q

myopathy clinical features

A
  • Progressive weakness (rapid or slow), usually proximal
  • Normal reflexes
  • Normal tone
  • Moderate wasting
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16
Q

causative agent of myopathy

A

genetic
inflammatory
metabolic

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17
Q

clinical features of myasthenia gravis

A
weakness
fatigability
worse as the day goes by
normal sensation
normal reflexes
repetitive nerve stimulation
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18
Q

muscle disease

A

myopathy

19
Q

example of neuromuscular junction disorder

A

myasthenia gravis

20
Q

causative agent of myasthenia gravis

A

any problem affecting receptors on muscles

21
Q

example of focal nerve pathology causing muscle weakness

A

carpal tunnel syndrome

22
Q

features of carpal tunnel syndrome

A

Pins and needles
Numbness
Pain in sensory distribution of median nerve (digit 1,2,3)
Worse at night
Weakness in motor part of median nerve
Reduced pin prick sensation
Very severe  weakness of muscles in median nerve region

23
Q

polyneuropathy

A

multiple peripheral nerves become damaged

24
Q

clinical features of polyneuropathy

A
Symptoms are more diffused like in upper and lower limb
Pins and needles
Numbness 
Burning sensation
Tingling
Weakness if motor nerves involved
25
Q

causes of polyneuropathy

A

diabetes

26
Q

example of root pathology causing muscle weakness

A

radiculopathy

27
Q

radiculopathy

A

pinching of nerve at spinal level

28
Q

clinical features of radiculopathy

A

Sensory and motor symptoms in distribution of specific nerve root
Back pain if lower spinal problem
Neck pain if upper spinal problem

29
Q

why is dorsal root ganglion spared in most spine pathologies

A

it lies outside the spinal cord

30
Q

how to differentiate between spinal nerve pathologies or root pathologies

A

normal sensory and electrodiagnostic tests for spine pathologies as dorsal root ganglion lies outside of the spinal cord

31
Q

motor neuron disease

A

disease of motor neurones (upper or lower or both)

32
Q

clinical features of motor neurone disease

A

Painless
Progressive Bulbar palsy –> weakness in the tongue and the face and the palate
Dysphasia, dysarthria, nasal regurgitation and aspiration
Progressive muscle weakness

33
Q

causes of motor neuron disease

A

sporadic

5-15% genetic

34
Q

two main electrodiagnostic tests

A
nerve conduction studies (NCS)
needle electromyography (EMG)
35
Q

nerve conduction study - 2 types

A

median nerve sensory study

median nerve motor study

36
Q

median nerve sensory study

A

Electrodes on hand and arm - along median nerve
At wrist = recording electrodes
On thumb = stimulatory electrodes
Stimulate median nerve at thumb and response will be recorded at the median nerve at the wrist

37
Q

median nerve motor study

A

Electrodes on small muscle in hand supplied by median nerve = abductor pollicis brevis
Stimulatory electrodes on median nerve
Electric stimulus to median nerve and response is recorded from abductor pollicis brevis on the screen
= compound muscle action potential seen on the screen

38
Q

Electromyography (EMG)

A

A fine needle is inserted in a muscle
We record from motor units in the muscle
Activate the muscle (in this case to flex the bicep, bend the elbow)
Motor unit action potentials
By looking and listening to this activity, we can differentiate between different pathologies

39
Q

EMG findings: Spontaneous activity

A

When we insert the needle – any activity which is recorded when muscle is relaxed and not stimulated
E.g., fibrillation potentials and positive sharp waves

40
Q

Motor unit

A

number of muscle fibres supplied by a single motor neuron

41
Q

EMG findings: recruitment / interference patterns - NORMAL

A

In a normal person, there should be a screen full of motor action potential when muscle is contraction - there should be no gaps

42
Q

EMG findings: recruitment / interference patterns - nerve problems / denervation

A

if there are gaps / reduced interference pattern

43
Q

EMG findings: recruitment / interference patterns - muscle problems

A

with less effort, the screen can be seen to be pull but MUAP is smaller