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Learn about Supranuclear ophthalmoplegia, find a doctor, complications, outcomes, recovery and follow-up care for Supranuclear ophthalmoplegia.
Progressive supranuclear palsy is a rare brain disease that affects walking, balance, eye movements and swallowing. The disease results from the damage of cells in areas of the brain that control body movement, coordination, thinking and other important functions.
Progressive supranuclear palsy (PSP) is a form of atypical parkinsonian syndrome, also known as a Parkinson-plus disorder. It is an uncommon neurological disorder that can affect movement, gait, balance, speech, swallowing, vision, eye movements, mood, behavior, and cognition.
Progressive supranuclear palsy (PSP) is a rare and chronic neurodegenerative disorder that damages certain areas of your brain. It affects how you walk, think, swallow and move your eyes. It may also cause other symptoms. PSP is also known as Steele-Richardson-Olszewski syndrome.
What is progressive supranuclear palsy? Progressive supranuclear palsy (PSP) is a rare neurological disorder that affects body movements, walking and balance, and eye movements. PSP is caused by damage to nerve cells in areas of the brain that control thinking and body movements.
Progressive supranuclear palsy (PSP) or Steele-Richardson-Olszewski syndrome is characterized by a progressive supranuclear ophthalmoplegia typically vertical but in particular downward limitation of eye movement.
Progressive supranuclear palsy can cause changes in your brain that make you feel anxious or laugh or cry for no reason. Progressive supranuclear palsy also can become frustrating as walking, talking and eating become harder.
Progressive supranuclear palsy (PSP) is a late-onset neurodegenerative disease involving the gradual deterioration and death of specific volumes of the brain. [2] [3] The condition leads to symptoms including loss of balance, slowing of movement, difficulty moving the eyes, and cognitive impairment. [2]
Progressive supranuclear palsy is a rare, degenerative central nervous system disorder that progressively impairs voluntary eye movements and causes bradykinesia, muscular rigidity with progressive axial dystonia, pseudobulbar palsy, and dementia. Diagnosis is clinical.
Symptoms. People with supranuclear ophthalmoplegia are unable to move their eyes at will in all directions, especially looking upward. Other symptoms may include: Mild dementia. Stiff and uncoordinated movements like those of Parkinson disease. Disorders associated with supranuclear ophthalmoplegia. Exams and Tests.