Week 11b: Disorders of Motor Function Flashcards

1
Q

Which type of motor neuron lesion?

  • paralysis affects movement rather than muscle
  • muscle wasting is only from disuse
  • spasticity of “clasping knife” type
  • muscles are hypertonic
A

upper motor neuron lesion

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2
Q

Which type of motor neuron lesion?

  • individual muscle or group of muscles affected
  • muscle wasting is pronounced
  • Flacidity
  • muscles are hypotonic
A

lower motor neuron lesion

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3
Q

What is characterized by a reduction in the diameter of the muscle fibres because of a loss of protein filaments

A

muscle atrophy

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4
Q

Disuse atrophy

A

result of a normally innervated muscle not being used for long periods. The cells shrink but do not die

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5
Q

progressive deterioration of skeletal muscles because of mixed muscle cell hypertrophy, atrophy and necrosis

A

muscular dystrophy

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6
Q

Muscular dystrophy probably does not involve?

A

the nervous system

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7
Q

pseudohypertophy

A

when fat and connective tissue replaces the muscle fibres which increases muscle size and results in muscular weakness

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8
Q

growers sign is associated with?

A

Duchenne muscular dystrophy

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9
Q

signs of muscle weakness associated with Duchenne muscular dystrophy become evident…?

A

beginning at 2-3 years, when frequent falling occurs

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10
Q

respiratory muscle involvement in Duchenne muscular dystrophy

A

results in a weak and ineffective cough and frequent respiratory infections

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11
Q

a disorder of transmission at the neuromuscular junction that affects communication between the motor neuron and the innervated muscle cell

A

myasthenia gravis

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12
Q

an autoimmune disease caused by antibody mediated loss of acetylcholine receptors in the neuromuscular junction

A

myasthenia gravis

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13
Q

what is the first noticeable sign of myasthenia gravis?

A

weakness of the eye muscles

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14
Q

other possible first symptoms of myasthenia gravis?

A
  • slurred speech

- difficult swallowing

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15
Q

other symptoms of myasthenia gravis that are variable in type and severity

A
  • ptosis
  • diplopia
  • unstable or waddling gait
  • change in facial expression
  • difficulty in swallowing
  • impaired speech (dysarthria)
  • weakness in arms, hands, fingers, legs and neck
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16
Q

myasthenia crisis

A

worsening of muscle weakness, resulting in respiratory failure that requires intubation and mechanical ventilation

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17
Q

the tension test assesses for?

A

myasthenia gravis

18
Q

what is important to have ready when administering the tension test?

A

atropine in case of bradycardia

19
Q

treatments of myasthenia gravis

A
  • cholinesterase inhibitors
  • corticosteroids
  • immunosuppressants
  • plasmapheresis
  • IVIg
  • monoclonal antibody
  • thymectomy
20
Q

Characteristics of disorders of the basal ganglia

A
  • involuntary movements
  • alterations in muscle tone
  • disturbances in body posture
21
Q

a degenerative disorder of basal ganglia function that results in variable combinations of tremor, rigidity and bradykinesia

A

PKD

22
Q

progressive destruction of the dopamine nigrostriatal pathway with subsequent reduction in striatal concentrations of dopamine

A

PKD

23
Q

Dopamine deficiency in the basal ganglia associated with motor impairment

A

PKD

24
Q

PKD results in difficulty…?

A

initiating and controlling movements

25
Q

permanent destruction of the myelin sheath of the CNS

A

MS

26
Q

Symptoms as MS progresses

A

paralysis, vision loss and diminished brain function

27
Q

a progressive motor disorder affecting upper motor neurons and lower motor neurons

A

MS

28
Q

MS disease susceptibility is linked to…?

A

the HLA locus on chromosome 6

29
Q

first stage of MS

A

inflammation and small lesions due to antibody-antigen reactions

30
Q

second stage of MS

A

due to demyelination and gliosis (scar tissue) which slows, blocks or distorts transmission impulses

31
Q

a disease that is more common in males, and is a degenerative disorder that involves UMN and LMN and progressive muscle wasting

A

ALS

32
Q

temporary loss or depression of all or most spinal reflex activity below the level of injury

A

spinal shock

33
Q

what is a possible complication of spinal shock?

A

hypotension due to the lack of sympathetic tone

34
Q

example of a drug that is a dopamine precursor for PKD

A

levodopa

35
Q

example of a drug that is a dopamine receptor agonist for PKD

A

mirapex

36
Q

example of a maoi for PKD

A

selegiline

37
Q

example of a drug that promotes the release of dopamine for PKD

A

amantadine and COMT inhibitors

38
Q

example of drugs that decrease the effect of Ach for PKD?

A

benztropine and diphenhydramine

39
Q

adverse effects of sinemet

A
  • orthostatic hypotension
  • nausea, vomiting, dysphagia, anorexia, flatulence
  • involuntary choreifrom movements
  • headaches, anxiety, depression, agitation, insomnia
40
Q

adverse effects related to anticholinergic meds

A
  • sedation, confusion
  • constipation
  • nausea and vomiting
  • blurred vision, dilated pupils
  • dry mouth, dry skin
  • urinary retention