Parkinson's Disease and Other Movement Disorders Flashcards

1
Q

what are the functions of the basal ganglia? (4)

A
  • connect the motor cortex with the midbrain
  • receive input from the neocortex, including the motor cortex and limbic cortex
  • receive from the nigrostriatal dopamine pathway from the substantia nigra
  • output back to the motor cortex and substantia nigra
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2
Q

what is the nigrostriatal pathway important for?

A

smooth movements

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3
Q

what are the subcomponents of the basal ganglia? (9)

A
  • caudate nucleus
  • putamen
  • globus pallidus pars interna (GPi)
  • globus pallidus pars externa (GPe)
  • subthalamic nucleus
  • substantia nigra pars compacta (SNc)
  • substantia nigra pars reticulata (SNr)
  • intralaminar thalamic nuclei
  • ventral pallidum
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4
Q

what causes Parkinson’s Disease? What does this result in?

A
  • caused by loss of dopamine cells in the substantia nigra and their input to the basal ganglia
  • results in muscular rigidity and difficulty initiating and performing movements
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5
Q

what are the symptoms associated with Parkinsonism? (4)

A
  • resting tremor
  • rigidity
  • akinesia (lack of movement) or bradykinesia (very slow movement)
  • postural instability
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6
Q

what are the characteristics of Parkinson’s Disease? (3)

A
  • typically idiopathic (no known cause)
  • Lewy Bodies in substantia nigra
  • have resting tremor, rigidity, bradykinesia, postural instability, hypophonia, masked facies, micrographic, shuffling gait, and stooped posture
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7
Q

what are the common neuropsychological deficits seen in PD? (6)

A
  • bradykinesia/bradyphrenia
  • visuoperceptual/visuoconstructional impairments
  • attention/executive impairments
  • memory problems (retrieval deficit)
  • intractable depression
  • Parkinson’s Disease Dementia
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8
Q

what does corticobasal degeneration cause? (3)

A
  • apraxia
  • alien limb
  • aphasia
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9
Q

what does progressive supranuclear palsy cause?

A

problems with gaze resulting in increased risk of falling

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10
Q

what are the characteristics of Huntington’s Disease? (3)

A
  • autosomal dominant disease
  • destroys cells in the caudate putamen
  • results in involuntary and exaggerated movements
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11
Q

what are the characteristics of Tourettes’s Syndrome? (2)

A
  • related to damage to the caudate putamen

- results in unwanted tics and vocalization

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12
Q

what do the caudate nucleus and putamen make up?

A

the striatum

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13
Q

what doe the putamen, globus pallidus pars interna, and globus pallidus pars externa make up?

A

the lentiform nucleus

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14
Q

indirect pathway

A

inhibits the action of the cortex (Parkinson’s)

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15
Q

direct pathway

A

excited action of the cortex (Huntington’s)

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16
Q

what are the treatment options for movement disorders? (3)

A
  • L-dopa (primarily for PD)
  • deep brain stimulation (insert probe into substantia nigra to cause more activity and increase movement)
  • ablation treatments (taking out some inhibitory pathways to help with movement)
17
Q

what are the signs that a patient might not do well after deep brain stimulation? (5)

A
  • signs of dementia
  • neuropsychological deficits prior to PD
  • hallucinations (not due to L-dopa)
  • poor health generally
  • smaller hippocampi