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