Movement Disorders Flashcards

1
Q

What is the difference between rigidity + spasticity

A

Spasticity is velocity-dependent

tone increases the faster you move it

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2
Q

What is apraxia

A

Loss of movement planning

  • Limb apraxia: fronto-parietal cortex
  • Gait apraxia: Frontal lobe + Frontal White matter
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3
Q

What is myoclonus

A

A brief jerk

  • associated with cortex
  • associated with late stage dementia
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4
Q

What is Dystonia

A

Sustained, abnormal tone + posture of a group of muscles

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5
Q

What are the core symptoms of Parkinson’s disease

A
  • Rigidity
  • Tremor
  • Bradykinesia
  • Postural instability

Presents assymetrically

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6
Q

What are the non-core features of Parkinson’s disease

A
  • Hypomimia
  • Micrographia
  • Loss of arm swing
  • Festination (shuffling gait)
  • Cogwheel rigidity
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7
Q

How do you diagnose Parkinson’s disease

A

Clinical diagnosis

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8
Q

What is the management of PD

A

Changes as disease progresses

  1. L. Dopa + Carbidopa
  2. Dopamine agonists (Cabergoline)
  3. Deep brain stimulation
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9
Q

What are some of the characteristic side effects of anti-PD drugs

A
  • ‘On-off’ effect: sudden freezing + unfreezing
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10
Q

What is drug-induced Parkinsonism

A

Parkinsonian signs caused by drugs

  • e.g. neuroleptics, CCBs, lithium, antiemetics
  • Symmetrical onset
  • Symptoms resolve upon drug withdrawal
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11
Q

What is Vascular Parkinsonism

A

Parkinsonism caused by vascular pathology

  • Rare
  • Stuttering evolution
  • Marked sparing of upper limbs
  • Changes shown on MRI
  • CVD risk factors present
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12
Q

What are the classifications of Dystonia

A

Primary Dystonia

  • No evidence of pathology
  • Presentation: old (focal), young (generalised)

Secondary Dystonia
- Due to underlying pathology

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13
Q

Name two causes of secondary dystonia

A
  • Wilson’s disease

- Drug-induced

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14
Q

Clinical features of dystonia

A

Can often be ‘aborted’ by specific sensory stimulation
- ‘sensory tricks’

Can be focal or generalised

  • Focal: e.g. writers cramp, torticollis
  • Generalised: e.g. generalised torsion dystonia

Can present as a tremor

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15
Q

Management of dystonia

A

Botox injections

- last for ~3 months

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16
Q

Huntington’s disease - Cause

A

Expanding trinucleotide repeat mutation

- autosomal dominant

17
Q

Huntington’s disease - Clinical features

A

Insidious onset: over 10-15 years

First: personality changes
- poor impulse control, irritability

Then: chorea, dementia, immobility

18
Q

Huntington’s disease - Prognosis

A
  • Incurable

- Most dead within 20 years of onset