L26 - muscle weakness Flashcards

(43 cards)

1
Q

UMN origin

A

primary motor cortex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

LMN origin

A

ventral horn of spinal cord

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

muscle tone of UMN causes of muscle weakness

A

increased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

reflexes in UMN causes of muscle weakness

A

increased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

plantars in UMN muscle weakness

A

increased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

muscle tone of LMN causes of muscle weakness

A

decreased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

reflexes in LMN causes of muscle weakness

A

decreased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

plantars in LMN muscle weakness

A

decreased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

causes of UMN muscle weakness

A

stroke
infection
tumour
degeneration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

clinical findings in UMN muscle weakness

A

weakness
mild atrophy
brisk reflexes
upping plantars

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

clinical findings in LMN muscle weakness

A

weakness
mild atrophy
depressed or absent reflexes
down going plantars

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

common LMN pathologies in muscle weakness

A
muscle
neuromuscular junction
nerve
root pathology
anterior horn
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

natures of LMN muscle weakness

A
  • axonal loss pathology

- demyelination pathology

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

myopathy clinical features

A
  • Progressive weakness (rapid or slow), usually proximal
  • Normal reflexes
  • Normal tone
  • Moderate wasting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

causative agent of myopathy

A

genetic
inflammatory
metabolic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

clinical features of myasthenia gravis

A
weakness
fatigability
worse as the day goes by
normal sensation
normal reflexes
repetitive nerve stimulation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

muscle disease

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
causes of polyneuropathy
diabetes
26
example of root pathology causing muscle weakness
radiculopathy
27
radiculopathy
pinching of nerve at spinal level
28
clinical features of radiculopathy
Sensory and motor symptoms in distribution of specific nerve root Back pain if lower spinal problem Neck pain if upper spinal problem
29
why is dorsal root ganglion spared in most spine pathologies
it lies outside the spinal cord
30
how to differentiate between spinal nerve pathologies or root pathologies
normal sensory and electrodiagnostic tests for spine pathologies as dorsal root ganglion lies outside of the spinal cord
31
motor neuron disease
disease of motor neurones (upper or lower or both)
32
clinical features of motor neurone disease
Painless Progressive Bulbar palsy --> weakness in the tongue and the face and the palate Dysphasia, dysarthria, nasal regurgitation and aspiration Progressive muscle weakness
33
causes of motor neuron disease
sporadic | 5-15% genetic
34
two main electrodiagnostic tests
``` nerve conduction studies (NCS) needle electromyography (EMG) ```
35
nerve conduction study - 2 types
median nerve sensory study | median nerve motor study
36
median nerve sensory study
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
median nerve motor study
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
Electromyography (EMG)
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
EMG findings: Spontaneous activity
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
Motor unit
number of muscle fibres supplied by a single motor neuron
41
EMG findings: recruitment / interference patterns - NORMAL
In a normal person, there should be a screen full of motor action potential when muscle is contraction - there should be no gaps
42
EMG findings: recruitment / interference patterns - nerve problems / denervation
if there are gaps / reduced interference pattern
43
EMG findings: recruitment / interference patterns - muscle problems
with less effort, the screen can be seen to be pull but MUAP is smaller