A) Complete lack of tremor B) Inability to walk C) Additional clinical features D) Age of onset exclusively under 30
A) Progressive supranuclear palsy B) Amyotrophic lateral sclerosis C) Multiple sclerosis D) Huntington's disease
A) Primary and secondary B) Synucleinopathies and tauopathies C) Genetic and metabolic D) Acute and chronic
A) Supranuclear gaze palsy B) Pick's disease C) Corticobasal degeneration D) Shy–Drager syndrome
A) Late-onset postural instability B) Unilateral tremor C) Symmetrical onset D) Excellent response to levodopa
A) MRI B) CT scan C) SPECT D) PET scan
A) Progressive supranuclear palsy B) Pick's disease C) Corticobasal degeneration D) Dementia with Lewy bodies
A) Ataxia and dysarthria B) Alien limb and apraxia C) Resting tremor and rigidity D) Memory loss and hallucinations
A) They are less likely to respond B) They respond significantly better C) They show identical response D) They react negatively to all medication
A) High-dose levodopa monotherapy B) Preventative gene therapy C) Multidisciplinary treatment of symptoms D) Curative surgery
A) Reduced axial muscle rigidity B) Increased dopamine production C) Supranuclear gaze palsy D) Spontaneous recovery
A) Reversible B) More slowly progressive C) Stable without progression D) More rapidly progressive |