Movement Disorders - Hon Flashcards

1
Q

2 types of movement disorders

A

Bradykinetic, Hyperkinetic

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2
Q

3 Cardinal signs of Parkinson’s

A

Resting tremor (fingers, mouth, or chin)
Rigidity to all movement
Bradykinesia (slow movement, difficulty initiating)

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3
Q

Parkinson’s vs. PSP

A

PSP = loss of voluntary vertical gaze

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4
Q

Parkinson’s vs. MSA

A

MSA = severe autonomic dysfunction

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5
Q

Parkonson’s vs. Cortical Basal Degeneration

A

CBD = cortical sensory loss, apraxia, myoclonus, aphasia

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6
Q

Do Parkinson-like diseases respond to anti-PD medications?

A

Not well

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7
Q

Anti-Parkinson treatments

A
Dopamine agonists (Bromocriptine)
Levodopa (Sinemet)
COMT inhibitors (COMTAN)
MAO-B inhibitors (Selegiline)
Anticholinergics (Benztropine, trihexylphenidyl)
Amantadine (anti-viral)
Surgery
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8
Q

Chorea

A

Brief, dance-like movements

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9
Q

Athetosis

A

Writhing, sinuous movements

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10
Q

Dystonina

A

Sustained muscle contractions that produce twisting and repetitive movements and abnormal postures

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11
Q

Ballism

A

Large-amplitude flinging movements (proximal extremity)

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12
Q

Tic

A

Brief, rapid, repetitive stereotyped actions of 1 or more muscle groups

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13
Q

Children/young people
Unilateral choreiform movements (like restlessness or fidgeting), behavioral changes, previous group A strep infection

Treatment?

A

Sydenham’s Chorea

Bedrest, antibiotics

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14
Q
Neck twisted to one side (torticollis)
Spontaneous involuntary forceful closure of eyelids
Spasms of mouth muscles
Arm and hand in "waiter's tip" position
Leg in extension, foot in inversion

Treatment?

A

Idiopathic Torsion Dystonia

Levodopa, anticholingergics, benzo’s, baclofen, carbamazepine

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15
Q

Idiopathic Torsion dystonia, but seemingly confined to ONE area

Additional medication?

A

Focal torsion dystonia

BOTOX injection

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16
Q

Childhood or young adult
Tremor, Choreiform movements, Rigidity, Bradykinesia, Dysarthria, dysphagia, Ataxia, Dementia, Psychosis/hallucinations

IOW, bradykinesia PLUS hyperkinesia symptoms

A

Wilson’s disease

Copper metabolism deficit

Autosomal recessive, Chromosome 3

17
Q

Diagnosis of Wilson’s disease

A

Increased copper in urine
Decreased serum cerruloplasmin
Kayser-Fleischer Ring on eye exam

18
Q

Treatment for Wilson’s disease

A

Penicillamine, restriction to dietary copper

19
Q

Chronic multiple motor (face, throat) and vocal (bark, hiss, grunt) tics
Imitation of other people’s movements or speech
Repitition of words or phrases
Child or teenager - MALE

Treatment?

A

Gilles De La Tourette’s Syndrome

Clonidine, Haldol, Phenothiazines

20
Q

Both hands tremor (resting or intention)
Head and voice can be included too
Seen later in life
Alcoholic?

Treatment?

A

Benign Familial Tremor (Essential Tremor)

Beta blockers (propranolol), Primidone, Benzo’s