61
February 2017Movement disorders, involuntary / tic disorders
Movement disorders are classified as excessive (hyperkinetic) or reduced (bradykinetic) activity. Diagnosis depends primarily on careful observation of the clinical features.
(list not exhaustive)
Hyperkinetic
Tics
Primary (sporadic and inherited)
Secondary
Dystonia
Primary (sporadic and inherited)
Dystonia plus syndromes (e.g., medication)
Stereotypies (typically with mental retardation or autism)
Chorea/Athetosis/Ballism
Essential tremor
Myoclonus
Bradykinetic
Parkinson disease
Wilson disease
Huntington disease
Tremor
Resting (e.g., Parkinson, severe essential)
Intention (e.g., cerebellar disease, multiple sclerosis)
Postural/Action (e.g., enhanced physiologic, essential)
Given a patient with a movement disorder, the candidate will diagnose the cause, severity and complications, and will initiate an appropriate management plan.
Given a patient with a movement disorder, the candidate will
list and interpret critical clinical findings, including
describing the abnormal movement accurately after careful observation (at rest and in action) to differentiate between various types and causes of movement disorders;
performing a history and physical examination to look for reversible causes (e.g., medications, Wilson disease);
identifying key physical findings characteristic of Parkinson disease (e.g., rigidity, akinesia);
list and interpret critical investigations including
testing for Wilson disease, if indicated;
imaging studies or other tests, as appropriate;
construct an effective initial management plan, including
initiating medications for common conditions (e.g., essential tremor);
recognizing side effects of medication and modifying as necessary (e.g., dystonia, “on/off” phenomenon);
determining if the patient requires specialized care for diagnosis or management (e.g., genetic testing);
counselling about the psychosocial impact of the disorder.