Lec 35 Hyperkinetic Movement Disorders Flashcards

1
Q

What is a tremor?

A
  • regular oscillatory movement around defined axis
  • has a frequency and amplitude
  • may occur at rest, with posture, or with kinetic movements
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is an essential tremor? cause?

A
  • action/posture tremor = get worse when you try to move affected area
  • exacerbated by holding posture/limb position
  • see in head, hands, voice, classically tremor in both hands
  • worsens over time, rest tremor may emerge
  • autosomal dominant inheritance pattern
  • pts often self-medicated with alcohol to decrease tremor amplitude

pathology: loss of purkinje cells in cerebellum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is treatment for tremor?

A
  • primidone [anticonvulsant]
  • botulinum toxin injection
  • beep brain stimulation in VIM of thalamus
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is dystonia?

A
  • slow, twisting, repetitive movements
  • sustained involuntary muscle contractions
  • worsens in certain postures
  • can partially alleviate movement by touching affected body part
  • maybe be focal or generalized
  • due to Da or ACh dysfunction in basal ganglia
    ex. writers cramp, blepharospasm [eyelid twitch]
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is DYT1 dystonia?

A
  • autosomal dominant
  • overrepresentation in ashkenazi jews
  • begins in legs and progresses
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is Dopa-responsive dystonia?

A
  • leg dystonia in young children that worsens lateral in the day
  • responsive to small doses of levodopa
  • due to mutation in GCH1 gene
  • not degenerative
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is tardive dystonia?

A
  • arises from treatment with medications that block dopamine receptors
  • lip smacking + pursing, tongue protrusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is rapid-onset dystonia and parkinsonism?

A
  • genetic etiology
  • begins abruptly in childhood
  • develop bradykinesia with dystonia in face/hands/legs
  • parkinsonism not responsible to levodopa
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is monoclonus-dystonia?

A
  • fast jerks of myoclonus + dystonia in neck, arms, trunk
  • can lead to falls when walking
  • myoclonus improves with alcohol
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is monoclonus?

A
  • sudden rapid shock-like muscle contractions
  • can be in isolation or as part of other neuro diseases
  • ex. hiccups, jerks, epliepsy, seen in renal and liver failure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is asterixis?

A
  • negative monoclonus –> brief loss then resumption of muscle contraction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is chorea? cause?

A
  • sudden irregular jerky purposeless movements
  • most common in distal extremities

chorea = dancing

due to lesion of basal ganglia [huntingon]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are 2 treatments for essential tremor?

A
  • primidone [anti-convulsant]

- beta blockers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is sydenham chorea?

A
  • chorea post strep infection

- usually self limited and does not require treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What causes huntingon disease/ pathophysiology?

A
  • autosomal dominant CAG expansion [>38 repeats] on chromosome 4
  • decreased GABA and ACh in brain, neuronal death via NBDA-R binding and glutamate toxicity
  • progressive atrophy of striatum [particularly caudate nuclei] on imaging
  • expansion of CAG repeats
    Caudate loses
    Ach and
    GABA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is presentation of huntington disease?

A
  • manifests age 20-50
  • present with
    1. chorea [starts clumsiness/fidgetiness], later get dysarthria, dysphagia, parkinsonism
    2. psych: aggression, depression
    3. dementia
    4. eye movments: slow saccade = early sign
17
Q

What is treatment for huntington?

A
  • no cure, only symptomatic treatment
  • dopamine antagonists [haloperidol] for psych
  • dopamine depleting agents for chorea
18
Q

What are tics?

A
  • unvoluntary production of movement/sound
  • premonition sensation, suppressible, suggestible
  • childhood onset –> occurs with OCD, ADHD in tourettes
19
Q

What is chorea ancanthocytosis?

A
  • oral-buccal movements and history of seizure in young adult with chorea
  • diagnose by presence abnormal erythrocytes on smear of peripheral blood
20
Q

What is an intention tremor? sign of what lesion?

A
  • slow zigzag motion when pointing/extending toward target

- sign of cerebellar dysfunction

21
Q

what is a resting tremor?

A
  • uncontrolled movement of distal appendages [hands]
  • occurs at rest, alleviated by intentional movement
  • characteristic of parkinsons
22
Q

What is pathogenesis of wilson’s disease?

A
  • autosomal recessive
  • inadequate hepatic copper secretion caused by mutation in ATP7B
  • causes copper accumulation in liver, blood, eye, brain –> progressive degeneration
23
Q

What is presentation/symptoms of wilsons?

A

Copper is Hella Bad

C: decreased ceruloplasmin, cirrhosis, corneal deposits [kaiser fleicher rings], carcinoma

H: hemolytic anemia

B: basal ganglia degeneration
–> parkinsonian symptoms

A: asterixis

D: dementia, dyskinesia, dysarthria

usually 10-25 yo presents with these

24
Q

If you see liver symptoms + neuro/psych symptoms what should you think?

A

Wilson’s disease

25
Q

What is treatment for wilsons disease?

A
  • penicillamine