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27 Cards in this Set

  • Front
  • Back
How are movement disorders broadly classified?
1. akinetic disorder - too little
2. hyperkinetic disorder - too much
Definition of Parkinsonism
Bradykinesia

Plus any of the followings:
1. rigidity
2. resting tremor
3. postural instability
Clinical classification of Parkinsonian disorders
1. Idiopathic Parkinson's disease
2. Parkinsonism- plus
3. Heredo-degenerative
4. Secondary
Parkinson's disease is a clinical diagnosis, what are the 3 steps in the Queen Square Brain Bank Criteria?
Step 1: parkinsonism
Step 2: exlusion criteria
Step 3: supportive criteria
Parkinson's disease is not just a motor disease, give some non-motor symptoms
1. anosmia
2. bradyphrenia (slow thinking)
3. dementia
4. autonomic dysfunction (late)
Give pathology of Parkinson's disease Give the pathological hallmark of this disease and the types of the hallmark
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
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
Give some possible environmental factors of Parkinson's disease
1. Neurotoxin
2. Diet (high fat, high calories)

Caffein, alcohol, smoking: inverse association
When should we delay the use of levodopa and why?
Delay if age < 60

dyskinesia more easily to develop.
Medical treatmnet for Parkinson's disease
+ve:
Dopamine agonists, levodopa

-ve:
MAO-B inhib, anticholinergic, NMDA inhib, COMT inhib, adenosine (2a) antagonist
Give some Parkinsonism- Plus disorders
1. Multiple system atrophy
2. Progressive supranuclear palsy
3. Cortico-basal degeneration
Give some Heredo-degenerative disorders
1. Wilson's disease
2. Huntington's disease
Give some secondary parkinsonian disorder
1. Infection
2. Trauma
3. Vascular disease
Give 3 clinical features of Multiple System Atrophy
1. autonomic dysfunction
2. parkinsonism
3. cerebellar dysfunction

Nocturnal stridor: late feature
Imaging of MSA
CT: infratentorial atrophy
MRI: putamen slit sign, hot-cross bun sign
Pathology of MSA
Glial cytoplasmic inclusions
Medical Mx of MSA
Levodopa ( parkinsonism, but unsustaned response)

Oxybutinin ( bladder urgency)

Treat orthostatic hypotension
Clinial features of Progressive Supranuclear Palsy
1. axial feature
-fall backwards
-loss of postural reflex
-axial regidity

2. bradykinesia
3. reptilian stare
4. imparied downgaze
5. swallowing difficulty
Pathology of Progressive Supranuclear Palsy
Nuerofibrillary tangles
Imaging of Progressive Supranuclear Palsy
MRI: dorsal midbrain atrophy
Medical Mx of Progressive Supranuclear palsy
Levodopa
Botulinum toxin (x retrocollis)
Concerning Cortico - basal degeneration.
Highly assymmetrical - progressive - akinetic-rigid syndrome
Give some basal ganglia signs of cortico-basal degeneration
1. Akinesia
2. Alien limb phenomenon
Imaging of cortico-basal degeneration
Asymmetrical frontal-parietal atrophy
Medical Mx for cortico-basl degeneration
Levodopa (x parkinsonism)
Clonazepam (x myoclonus , action tremor)

Baclofen (x rigidity)

Botulinum toxin (x painful dystonia)
Give some hyperkinetic disorders
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
Tx of psychogenic movement disorder
1. avoid confrontation
2. psychotherapy