Movement Disorders Flashcards
Tremor
rhythmic oscillatory movement produced by alternating or synchronous contraction of antagonist muscles.
•Position when it happens the most? Resting, action (intentional), postural?
•Frequency? Slow or fast → PD tremor → 6 Hz
•Regular or jerky
Dystonia
- Focal (blepharospasm—eyes, hemifacial spasm, oromandibular dystonia, laryngeal dystonia, spasmodic torticolis/cervical dystonia), segmental, multifocal or generalized.
- Can be task-specific
- Duration: mobile, static, task specific.
Atheotosis
Slow, distal twisting movement
Myoclonus
Sudden brief, shock-like movement
Ataxia
Poorly coordinated, clumsy movement
Essential Tremor
Tremor with posture and action. Affects UE>LE and head
Insidious onset, progresses with age
Can cause degeneration
Familial and idiopathic. Unknown pathogenesis
Treatment: Primidone (anti-epileptic), Propranolol, Topamax (anti-epileptic)
Surgery (Thalamic deep brain stimulation
Postural Tremor
Emergent postural tremor; tremor kicks in after 30 sec or more
Usually associated with PD
Caused by loss of dopaminergic neurons in the direct and indirect pathways
Treatment: Sinemet (L-DOPA + Carbidopa), Dopamine receptor agonists, Amantidine, Anticholinergic drugs, MAO/COMT Inhibitors, Deep brain stim
Chin Tremor
Invariable facial expression
Usually assoicated with PD
Loss of dopaminergic neurons in the direct and indirect pathways
Treatment: Sinemet (L-DOPA + Carbidopa), Dopamine receptor agonists, Amantidine, Anticholinergic drugs, MAO/COMT Inhibitors, Deep brain stim
“Flapping Tremor” asterixis
Hold arms up with palms forward and tell patients to “stop”- see tic of hands
Not frequent, seen mostly in young people
Assicated with Wilson’s Disease, liver failure, uremia/kidney failure
Can be caused by copper accumulation in the lentiform nucleus causing basal ganglia degeneration
Treatable with chelating agents such as penicillamine
Tics
Brief, intermittent movements or sounds that are sudden, abrupt or transient. Repetitive, coordinated. Vary in intensity. Repeated at irregular intervals. May resemble gestures or normal behavior. Sometimes suppressible.
Associated with Tourette Syndrome
SLITRK1 Gene on chromosome 13. AD in other cases. Otherwise idiopathic
Treatment with Clonidine, SSRIs (for OCD), Neuroleptics, Tetrabenazine, Clonazepam
Chorea
Irregular, brief, dancing-like, jerky movements. Move from one body part to another
Associated with Huntington’s.
Sydenham chorea is the most common type in kids. Caused by post-strep immune reaction
Associated with Lupus»_space; 3rd most common neurologic presentation of Lupus
Dystonia
Contraction of muscle agonists and antagonists. Sustained muscle contractions cause twisting, abnormal posture.
Can be associated with tremor
Primary etiology is DYT 1-12.
Secondary etiology is from many causes, including neurodegenerative disorders, Ischemic brain injury, PTSD, Meds, Toxins
Botox helps a lot!
Tourette Sydrome
•Age of onset
Progressive supranuclear palsy
- Progressive
- Onset > 50 years old
- Impaired eye movements: can’t look down
- Reptilian or scared look
- Falls within the first year
Motor symptoms in Parkinson’s Disease
- Resting tremor
- Bradykinesia or akinesia
- Rigidity
- Non motor symptoms: autonomic instability, sleep disturbances