Progressive Supranuclear Palsy

Progressive supranuclear palsy (PSP) is a rare brain disease. It causes problems with balance, eye movement, and walking. Learn about what can help.

This content is for informational purposes only. Always consult a healthcare professional.
ⓘ Information

Before we begin: Progressive supranuclear palsy (PSP) is a rare brain disease. It causes problems with balance, eye movement, and walking. Learn about what can help.

This tutorial walks you through everything you need to know about progressive supranuclear palsy. We explain it in plain language, step by step, so whether you are a student, a patient, or simply curious, you will come away with a solid understanding.

We cover what it is, why it matters, how it is diagnosed, and what you can do about it. Key facts are called out along the way.

What is progressive supranuclear palsy (PSP)? Progressive supranuclear palsy (PSP) is a rare brain disease. It happens because of damage to nerve cells in the brain. PSP affects your movement, including control of your walking and balance. It also affects your thinking and eye movement.

PSP is progressive, which means that it gets worse over time.

What causes progressive supranuclear palsy (PSP)? The cause of PSP is unknown. In rare cases, the cause is a mutation in a certain gene.

One sign of PSP is abnormal clumps of tau in nerve cells in the brain. Tau is a protein in your nervous system, including in nerve cells. Some other diseases also cause a buildup of tau in the brain, including Alzheimer’s disease.

Who is at risk for progressive supranuclear palsy (PSP)? PSP usually affects people over 60, but in some cases it can start earlier. It is more common in men.

What are the symptoms of progressive supranuclear palsy (PSP)? Symptoms are very different in each person, but they may include:

A loss of balance while walking. This is often the first symptom.

Speech problems

Trouble swallowing

A blurring of vision and problems controlling eye movement

Changes in mood and behavior, including depression and apathy (a loss of interest and enthusiasm)

Mild dementia

How is progressive supranuclear palsy (PSP) diagnosed? There is no specific test for PSP. It can be difficult to diagnose, because the symptoms are similar to other diseases such as Parkinson’s disease and Alzheimer’s disease.

To make a diagnosis, your health care provider will take your medical history and do physical and neurological exams. You may have an MRI or other imaging tests.

What are the treatments for progressive supranuclear palsy (PSP)? There is currently no effective treatment for PSP. Medicines may reduce some symptoms. Some non-drug treatments, such as walking aids and special glasses, may also help. People with severe swallowing problems may need gastrostomy. This is a surgery to insert a feeding tube into the stomach.

PSP gets worse over time. Many people become severely disabled within three to five years after getting it. PSP isn’t life-threatening on its own. It can still be dangerous because it increases your risk of pneumonia, choking from swallowing problems, and injuries from falling. But with good attention to medical and nutritional needs, many people with PSP can live 10 or more years after the first symptoms of the disease.

NIH: National Institute of Neurological Disorders and Stroke

Also known as: PSP, Richardson-Steele-Olszewski syndrome, Steele-Richardson-Olszewski syndrome.

Related topics: Steele-Richardson-Olszewski Syndrome.

Categories: Brain and Nerves.

Source: National Institutes of Health — National Institute of Neurological Disorders and Stroke.

Key Takeaways

Understanding progressive supranuclear palsy is an important part of taking charge of your health. Here is what to remember:

  • Know the signs — Recognizing early symptoms can lead to earlier diagnosis and better outcomes.
  • Talk to your provider — If you have concerns or a family history of this condition, bring it up at your next checkup.
  • Stay informed — Medical knowledge evolves. Keep learning and asking questions.
  • You are not alone — Many people deal with this condition. Support groups and educational resources can help.
⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional for diagnosis and treatment of any medical condition.