Movement Disorders Flashcards

1
Q

Define tremor

A

Fine stereotyped oscillation

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2
Q

Define chorea

A

Medium speed complicated moves

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3
Q

Define athetosis

A

Slow complicated movements

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4
Q

Define ballism

A

Fast complicated movements (violent flinging of limbs)

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5
Q

Define tics

A

Jerk like very brief repetitive movements

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6
Q

Is glutamate excitatory or inhibitory?

A

Excitatory

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7
Q

Is dopamine excitatory or inhibitory?

A

Either excitatory to D1 receptors or inhibitory to D2 receptors

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8
Q

Is GABA excitatory or inhibitory?

A

Inhibitory

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9
Q

Principle defect in Parkinson’s disease?

A

Loss of dopamine in substantia nigra of basal ganglia

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10
Q

Basic features of Parkinson’s disease

A
  1. Rigidity
  2. Tremor at rest (3-5 Hz pill rolling)
  3. Bradykinesia
  4. Loss of postural reflexes
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11
Q

How does Parkinson’s generally present early on?

A

Begins in one limb and spreads asymmetrically

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12
Q

What are the most diagnostic features of PD?

A

Rigidity and bradykinesia

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13
Q

Is it ok to delay treatment of PD?

A

Yes - meds are symptomatic not neuroprotective

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14
Q

What is the most effective medication option for PD?

A

Carbidopa/Levodopa (Sinemet)

-Replaces presynaptic dopamine

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15
Q

Which dopamine agonists are post-synaptic?

A
  • Ropinirole (Requip)
  • Pramipaxole (Mirapex)
  • Pergolide (Ergot family)
  • Bromocryptine (Ergot family)
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16
Q

Define parakinesia

A

Cover up movement to make a choreiform movement look purposeful

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17
Q

Describe Huntington’s disease

A

Autosomal dominant neurodegenerative disease with chorea, dementia, personality disorder

18
Q

Main traits of Huntington’s disease

A
  1. Chorea
  2. Dementia
  3. Personality disorder
19
Q

Genetic feature of Huntington’s

A

CAG trinucleotide repeat (which makes longer than normal proteins)

20
Q

What is the MC movement disorder?

21
Q

Types of tremor

A
  • Resting (as in Parkinson’s, 3-5 Hz)
  • Intention/Kinetic
  • Essential (8-11 Hz, worse w/caffeine, better w/ETOH, bilateral)
22
Q

Define tremor

A

Rhythmic involuntary movement

23
Q

Features of Tardive Dyskinesia

A
  • Repetitive purposeless movements often of the face (but can be on trunk or limbs)
  • Tongue rolling, lip smacking
24
Q

Etiology of Tardive Dyskinesia

A

Usually iatrogenic - prolonged use of dopamine blockers (psych pts, diabetics w/gastroparesis)

25
Is tardive dyskinesia hypo or hyperkinetic?
Hyperkinetic
26
Define myoclonus
- Hyperkinetic disorder | - Involuntary sudden shocklike muscle jerks
27
Etiology of myoclonus
Usually CNS insult - anoxic/ischemic/alcoholics
28
Define restless leg syndrome
- Neuro movement disorder of the limbs often a/w sleep | - Mostly mild symptoms and do not need treatment
29
Diagnosis of RLS
4 core symptoms: - Urge to move legs bc of irritating sensation - Worse at rest - Relief w/movement - Worse at night
30
Treatment of primary RLS
- Dopamine agonists (pramipexole, ropinirole) - Benzos - Anticonvulsants
31
Treatment of secondary RLS
Correct underlying disorder (anemia, TSH, B12, DM)
32
Define ataxia
Inability to coordinate muscle activity during voluntary movement
33
Pathophys of ataxia
- Degeneration of cerebellum | - Disease or damage to spinal cord and/or peripheral nerves
34
What does a positive Romberg indicate in relation to ataxia?
Ataxia is sensory in nature
35
Pure cerebellar lesions cause ____
Hyporeflexia
36
Any disturbance of sensory or motor function will cause ____
Ataxia
37
Mid-line cerebellar lesions cause ______
Gait and trunk instability
38
Lateral cerebellar lesions show (ipsilateral/contralateral?) to the pathology
Ipsilateral
39
What clinical sign is seen with cerebellar lesions (sometimes as the major physical feature)?
Nystagmus
40
What is the MC cause of ataxia in older age groups (acute/non traumatic/non toxic etiology)?
Wallenberg stroke
41
Describe Wallenberg stroke
Lateral medullary syndrome - Ipsilateral ataxia - Horner's - Pharynx dysfunction - MOTOR AND COGNITIVE INTACT