Movement Disorders Flashcards
Huntington’s Disease
Genetic AD-needed to diagnose
chorea and dementia
Circuit anatomy and physiology
Loop
- Starts at motor cortex
- Then to basal ganglia
- Back to motor cortex
- Final motor output: pyramidal and other tracts
Subthalamic nucleus linked to globus pallidus Substantia nigra (dopamine outputs)
Parkinsons patho
dopamine output to putamen is problem
3 core features Parkinsons
- slowness (bradykinesia)
- shaking (tremor: resting)
- stiffness (rigidity-cogwheel)
- Postural hypotension
Description Parks
Older patient Starts unilateral, tremor in one hand Degenerative No UMN signs Responds to L-dopa
Non-motor features Parkinsons
- REM Behaviour Disorder
- Hyposmia
- Constipation
- Hypersomnia
- Pain
- Depression/Anxiety
Bradykinesia:
Loss of automatic movements shuffling gait freezing gait masked facies small hand writing finger tapping test slow
Rigidity
Poor arm swing, flexed posture, freezing gait
Resting tremor
Pill rolling
STOPS WITH ACTION
Gait
Festinating
Other neurological disorders that have parkinsonism
Multi-system atrophy
Progressive supranuclear palsy
other degen
other metabolic
Drug management Parkinsons
anti-cholinergic (treats tremor)
main: increase dopamine via L-dopa (given with enzyme inhib to concentrate the production of dopamine in CNS instead of blood)
dopamine agonists
Non drug management Parks
constipation
acting out ones dreams: RBD
Physical exercise
Huntingtons
Too much dopamine
hyperkinetic movement disorder
chorea: fast, jerky, semipurposeful movements: face, limbs, trunk , gait
Looks fidgety and dystonic (grimace)
May look ataxic (but not actually coordination problem)
Can’t keep arms in steady extension or maintain a protruded tongue
How many trinucleotide repeats in Huntingtons
More than 39
Autosomal Dominant
European
Chorea initially (facial tics, grimacing, dancing feet), then motor problems
Psychiatric behavioural problems, paranoia and hallucinations then dementia