CM: Movement Disorders Flashcards

1
Q

What is parkinsonism?

A

clinical syndrome w several components: bradykinesia, tremors at rest, rigidity, stooped posture, shuffling gait, postural instability

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2
Q

What is bradykinesia/akinesia?

A

slowness of movement, absence or paucity of spontaneous movement and/or decreased amplitude

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3
Q

What is a tremor?

A

rhythmic oscillation of any body part, amplitude varies but frequency predictable

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4
Q

What are the different kinds of tremors?

A

essential, rest, dystonic, task-specific

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5
Q

What is Parkinson Disease?

A

neurodegenerative disorder characterized by paucity or slowness of movements and rest tremor
also has flexed posture, freezing, asymmetrical onset

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6
Q

How can Parkinson dz be diagnosed?

A

bradykinesia and 1 of the following: rigidity, rest tremor, postural instability (appears later)
exclude other etiologies

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7
Q

What are non-motor symptoms of Parkinson’s dz?

A

REM behavior disorder, cognitive disorders, autonomic dysfunction, GI and GU symptoms, sexual dysfunction, sensory symptoms (restless leg), fatigue

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8
Q

What is the pathogenesis of Parkinson’s dz?

A

less inhibition of SN –> more inhibition of thalamus –> less activation of cortex

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9
Q

When is levodopa used as treatment for Parkinson’s?

A

initiated when symptoms are “disabling”

complications = side effects, motor fluctuations, dyskinesia

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10
Q

When are DOPA agonists used as treatment for Parkinson’s?

A

early onset therapy, less effective long term, more side effects in older patients (sudden somnolence, hallucinations, edema, compulsive behaviors)

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11
Q

What are the features of surgical management of PD?

A

motor symptoms not optimally controlled: on-off fluctuations, significant dyskinesias
no evidence of cognitive decline
includes deep brain stimulation of STN or GPi

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12
Q

What are the features of DBS in PD?

A

doesn’t cure
bilateral needed for gait
smooths out on-off fluctuations, improves tremor, rigidity, dyskinesia
akinesia and postural instability responds least
programming requires frequent diligent follow up
decreases meds, doesn’t eliminate them

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13
Q

How can essential tremor be recognized?

A

progressive action tremor: postural + kinetic
bilateral: may involve head, voice, limbs
absence of other progressive neurological signs
may be mitigated by alcohol
torpedoes = swelling of proximal purkinje cells in cerebellum

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14
Q

What is dystonia?

A

abnormal muscle contraction causing sustained posture, co-contraction of agonist-antagonists
interrupts and is induced by limb movement
may cause repetitive tremor-like contractions

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15
Q

What are the different types of dystonia?

A

focal or generalized
idiopathic = primary cervical dystonia
drug induced = acute dystonia, tardive dystonia
genetic = primary torsion, dopa-responsive, Wilson’s dz
blepharospasm = eye closure

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16
Q

What is chorea?

A

non-rhythmyic, abrupt, unsustained
writhing, flowing, dance-like
random, unpredictable timing
focal or generalized

17
Q

What is ballism/hemiballism?

A

proximal, large amplitude, hemibody movements from lesion of contralateral STN/basal ganglia

18
Q

What is dyskinesia?

A

abnormal, involuntary, hyperkinetic movements

nonspecific

19
Q

What is stereotypy?

A

repetitive, usually continuous movements
fragments of normal movements
autism, rett disorder, mental retardation

20
Q

How can tardive dyskinesia be recognized?

A

persistent abnormal involuntary movements
face, mouth, lip sterotypies (chewing movements, tongue protrusion)
choreiform movements of limbs
pelvic thrusting, dystonia

21
Q

How can Wilson’s dz be recognized?

A

high serum and urine copper, low ceruloplasmin
neurological: tremor, drooling, dystonia, parkinsonian syndrome, cognitive impairment, dementia, psychosis
giant panda sign in midbrain

22
Q

How can Sydenham dz be diagnosed?

A

usually after group A beta hemolytic strep
chorea (hemi, of distal extremities), hypotonia, tics, behavioral abnormalities
elevated anti-streptolysin O, DNA-ase B titers

23
Q

What is the clinical triad of Huntington’s?

A

chorea and other movement abnormalities, cognitive (dementia, executive dysfunction), psychiatric (personality changes, depression, disinhibition, OC, addiction)

24
Q

What is myoclonus?

A

non-rhythmyic, abrupt, unsustained, rapid jerk-like

random unpredictable timing

25
Q

What is a tic?

A

recognizable pattern, unpredictable timing

urge –> tic –> transient relief –> urge –> tic…

26
Q

How can Tourette’s syndrome be diagnosed?

A

multiple motor and phonic tics
occur many times a day for at least 1 yr
onset before 21, no other explanation

27
Q

What is the pathophysiology of Huntingtons?

A

AD
CAG repeats >40
>60 = juvenile form