Diagnosing Weakness Flashcards

1
Q

What are the 2 functions of the upper motor neurone?

What happens if the UMN dies?

A
  1. start the message
  2. stop the message

if the UMN dies, the muscle does not know how to stop, as the message continues

this results in increased tone - spasticity

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2
Q

What are the different levels of weakness?

A
  • neurologically unexplained
  • upper motor neurone
  • lower motor neurone
  • neuromuscular junction
  • muscle fibre
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3
Q

What part of the brain / spinal cord is damaged if there is weakness on one half of the body / all four limbs / both legs / one limb?

A
  • one half of the body - cerebral hemisphere
  • all four limbs - high cervical spinal cord
  • both legs - low cervical spinal cord
  • one limb - spinal root or peripheral nerve
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4
Q

What pattern of weakness is present in generalised distal weakness and generalised proximal weakness?

A
  • generalised distal weakness - peripheral neuropathy
  • generalised proximal weakness - myopathy myasthenia
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5
Q

What is meant by monoplegia, hemiplegia, diplegia and quadriplegia?

A

monoplegia:

  • affects one limb only - usually an arm

hemiplegia:

  • affects one side of the body including arm, leg and trunk

diplegia:

  • affects symmetrical parts of the body (arms or legs)

quadriplegia:

  • affects all four limbs
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6
Q

What are the 4 stages involved in investigating weakness?

A

1 - history:

  • explore the symptoms
  • what? where? how long?

2 - examination:

  • clinical findings
  • muscle volume, strenght, tone, reflexes, involuntary movements

3 - tests:

  • genetics, pathology (biopsy and imaging)
  • looking for gene defects or abnormal muscle structure

4 - function:

  • EMG and NCS
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7
Q

What are the causes and clinical findings of an upper motor neurone problem?

A

causes:

  • stroke
  • infection
  • tumour
  • degeneration

clinical findings:

  • brisk reflexes
  • pathological reflexes
  • mild atrophy
  • stiffness
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8
Q

WHat are the causes and clinical findings of a lower motor neurone disorder?

A

causes:

  • infection
  • toxin
  • radiation
  • degeneration
  • trauma

clinical findings / localisation:

  • anterior horn
  • radiculopathy
  • two or more nerves
  • generalised peripheral neuropathy
  • single nerve injury
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9
Q

What are the signs of a LMN axonal lesion?

A
  • weakness +/- numbness
  • reduced relflexes
  • muscle wasting
  • fasciculation
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10
Q

What are the 2 main conditions affecting the neuromuscular junction?

A
  • myasthenia
  • myasthenic syndrome
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11
Q

What are the symptoms and signs of a problem at the neuromuscular junction?

A
  • proximal weakness
  • fatigability
  • worse as the day goes by
  • normal sensation
  • normal reflexes
  • repetitive nerve stimulation (RNS)
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12
Q

What are the 2 main disorders resulting from problems with muscle fibres?

A
  • myopathy
  • myositis
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13
Q

What are the symptoms and signs of muscle disease?

A
  • progressive weakness - usually proximal
  • normal sensation
  • normal reflexes
  • normal tone
  • moderate wasting
  • can be congenital, inherited, metabolic, toxic or mitochondrial
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14
Q

What is motor neurone disease?

What causes it?

A

a disease of motor neurones which is progressive

  • can be idiopathic (unknown cause)
  • 5-10% cases have a genetic cause (familial basis)
  • can be caused by toxins, viruses, trauma or combinations
  • tends to be sporadic (here and there)
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15
Q

Where do UMN and LMNs originate?

A

UMN originate in frontal motor gyrus - brainstem and spinal cord

LMNs have their cell bodies in the spinal cord

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16
Q

What happens in ALS?

A

Cells in the CNS and PNS start dying and there is cellular apoptosis

the lysosomes then digest the cells

17
Q

What are the symptoms and signs of motor neurone disease?

A
  • painless
  • no loss of feeling
  • progressive bulbar palsy - weakness in the tongue, the face and the palate
  • dyphasia
  • dysarthria
  • nasal regurgitation and aspiration
18
Q

What is life expectancy with MND?

Which functions are preserved in this condition?

A

life expectancy is 3-5 years - it is progressive with no remission

  • normal cognition
  • eye muscles are preserved
  • sphincter function is preserved
  • sexual activity is preserved
19
Q

What are the different clinical forms of MND?

A
  • progressive muscular atrophy (PMA)
  • primary lateral sclerosis (PLS)
  • progressive bulbar palsy (PBP)
  • MND - FTD
20
Q

How are EMG and NCS performed?

A

UMN - LMN - muscle

21
Q

What is invovled in generating a nerve impulse and it travelling to form a spinal nerve?

A
  • impulse generated in the cortex and passed to the anterior horn cell via CST or CBT
  • LMN exits the spinal cord forming ventral rootlets
  • the body of the sensory neurone lies in the dorsal ganglion
  • dorsal ganglion has a peripheral arm and the axon, which travels all the way to the brainstem
  • the dorsal and ventral roots come together to form spinal nerves
22
Q

What features of the motor system can be measured?

A
  • amplitude
  • duration
  • latency
  • conduction velocity
  • F-wave
23
Q
A