a progressive neurological disorder usually starting in the 6th decade of life and characterized by
oculomotor palsy, with downward gaze particularly affected. The condition may be accompanied by
parkinsonism, postural instability, speech and swallowing difficulties,
dystonia, personality changes, and typically mild cognitive impairment. Pathology often shows loss of neurons and
gliosis in various regions of the brainstem, basal ganglia, and midbrain. Also called
Steele–Richardson–Olszewski syndrome;
supranuclear palsy.