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27 Cards in this Set
- Front
- Back
How are movement disorders broadly classified?
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1. akinetic disorder - too little
2. hyperkinetic disorder - too much |
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Definition of Parkinsonism
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Bradykinesia
Plus any of the followings: 1. rigidity 2. resting tremor 3. postural instability |
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Clinical classification of Parkinsonian disorders
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1. Idiopathic Parkinson's disease
2. Parkinsonism- plus 3. Heredo-degenerative 4. Secondary |
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Parkinson's disease is a clinical diagnosis, what are the 3 steps in the Queen Square Brain Bank Criteria?
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Step 1: parkinsonism
Step 2: exlusion criteria Step 3: supportive criteria |
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Parkinson's disease is not just a motor disease, give some non-motor symptoms
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1. anosmia
2. bradyphrenia (slow thinking) 3. dementia 4. autonomic dysfunction (late) |
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Give pathology of Parkinson's disease Give the pathological hallmark of this disease and the types of the hallmark
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Pathology:
1. Dopaminergic neurons in substantia nigra pars compacta (SNpc) degenerate 2. exponential neuron loss 3. neuronal loss start at lat. part of ventral tier of SNpc Pathological hallmark: Lewy bodies 1. brainstem type 2. cortical type |
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Pathogenesis of Parkinson's disease
and the underlying chemical mechanism causing it |
1. Most sporadic
2. If age < 50, then significant enetic Central mechanism: 1. toxic proteins 2. oxidative stress |
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Give some possible environmental factors of Parkinson's disease
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1. Neurotoxin
2. Diet (high fat, high calories) Caffein, alcohol, smoking: inverse association |
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When should we delay the use of levodopa and why?
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Delay if age < 60
dyskinesia more easily to develop. |
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Medical treatmnet for Parkinson's disease
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+ve:
Dopamine agonists, levodopa -ve: MAO-B inhib, anticholinergic, NMDA inhib, COMT inhib, adenosine (2a) antagonist |
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Give some Parkinsonism- Plus disorders
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1. Multiple system atrophy
2. Progressive supranuclear palsy 3. Cortico-basal degeneration |
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Give some Heredo-degenerative disorders
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1. Wilson's disease
2. Huntington's disease |
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Give some secondary parkinsonian disorder
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1. Infection
2. Trauma 3. Vascular disease |
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Give 3 clinical features of Multiple System Atrophy
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1. autonomic dysfunction
2. parkinsonism 3. cerebellar dysfunction Nocturnal stridor: late feature |
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Imaging of MSA
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CT: infratentorial atrophy
MRI: putamen slit sign, hot-cross bun sign |
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Pathology of MSA
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Glial cytoplasmic inclusions
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Medical Mx of MSA
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Levodopa ( parkinsonism, but unsustaned response)
Oxybutinin ( bladder urgency) Treat orthostatic hypotension |
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Clinial features of Progressive Supranuclear Palsy
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1. axial feature
-fall backwards -loss of postural reflex -axial regidity 2. bradykinesia 3. reptilian stare 4. imparied downgaze 5. swallowing difficulty |
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Pathology of Progressive Supranuclear Palsy
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Nuerofibrillary tangles
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Imaging of Progressive Supranuclear Palsy
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MRI: dorsal midbrain atrophy
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Medical Mx of Progressive Supranuclear palsy
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Levodopa
Botulinum toxin (x retrocollis) |
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Concerning Cortico - basal degeneration.
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Highly assymmetrical - progressive - akinetic-rigid syndrome
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Give some basal ganglia signs of cortico-basal degeneration
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1. Akinesia
2. Alien limb phenomenon |
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Imaging of cortico-basal degeneration
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Asymmetrical frontal-parietal atrophy
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Medical Mx for cortico-basl degeneration
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Levodopa (x parkinsonism)
Clonazepam (x myoclonus , action tremor) Baclofen (x rigidity) Botulinum toxin (x painful dystonia) |
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Give some hyperkinetic disorders
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1. tremor ( rhythmic)
2. myoclonus ( sudden brief jerky, involuntary) +ve: contraction -ve: cessation of contraction --------------------------------------------------- 3. ballismus (violent flinging of entire limb) 4. chorea (rapid irreggular jerks) 5. athetosis (slow, flowing, twisting movement, distally) 6. dystonia (co-contraction) --------------------------------------------- 7. tics (recurrent, stereotyped) -simple: 1 muscle group -complex: cooridnated, sequenced 8. psychogenic movement disorder |
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Tx of psychogenic movement disorder
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1. avoid confrontation
2. psychotherapy |