How long can you live with progressive supranuclear palsy?

With good care and attention to medical needs, nutritional needs, and safety, a person with PSP can live many years. The typical lifespan from first appearance of symptoms is about 6-10 years. The main causes of death are infections and breathing problems.

What part of the brain does PSP affect?

Progressive supranuclear palsy (PSP) – or Steele-Richardson-Olszewski syndrome – is a rare neurodegenerative disorder that damages your brain (particularly the basal ganglia, substantia nigra, subthalamic nucleus, pars reticulata and other midbrain structures) and affects how you walk, think, swallow and move your eyes …

What is the final stage of PSP?

End of life stage: This stage is difficult to detect, but may be indicated by reduced levels of consciousness, inability to eat or drink, acute infection, a fall or major fracture, and rapid and significant weight loss. The end of life stage typically spans 6-8 weeks.

Can Bell’s palsy cause dementia?

About 1 in 10 people who have PSP have symptoms related to thinking and perception when they are diagnosed. However, about 7 in 10 people who have PSP are likely to develop dementia at some point. Although memory is not often badly affected by the condition, PSP can affect other parts of a person’s thinking.

What is PST disease?

Progressive supranuclear palsy is an uncommon brain disorder that causes serious problems with walking, balance and eye movements, and later with swallowing. The disorder results from deterioration of cells in areas of your brain that control body movement, coordination, thinking and other important functions.

Is PSP hereditary?

Progressive supranuclear palsy (PSP) is usually sporadic (not inherited ), but in rare cases it can be inherited. While the genetic cause of PSP not usually known, it can be caused by a mutation in a gene called MAPT.

What do you need to know about progressive supranuclear palsy?

Progressive supranuclear palsy (PSP) is an uncommon brain disorder that affects movement, control of walking (gait) and balance, speech, swallowing, vision, mood and behavior, and thinking.

How is Tau associated with progressive supranuclear palsy?

The protein tau is associated with microtubules – structures that support a nerve cell’s long processes, or axons, that transmit information to other nerve cells. The accumulation of tau puts PSP in the group of disorders called the tauopathies, which also includes other disorders such as Alzheimer’s disease,…

What does it mean when you have progressive eye palsy?

The disorder’s long name indicates that the disease worsens ( progressive) and causes weakness ( palsy) by damaging certain parts of the brain above nerve cell clusters called nuclei ( supranuclear). These nuclei particularly control eye movements.

Which is more progressive PSP or Parkinson’s disease?

Both PSP and Parkinson’s disease cause stiffness, movement difficulties, and clumsiness, but PSP is more rapidly progressive as compared to Parkinson’s disease.