Supranuclear Palsy
Supranuclear palsy (SPS), also known as progressive supranuclear palsy, is a rare brain disorder that causes serious problems with walking, balance, and eye movements.
Causes and Risk Factors
The exact cause of SPS is not fully understood, but it is believed to be related to the accumulation of abnormal tau protein in the brain. This leads to the degeneration of brain cells, particularly in the areas responsible for movement control.
Risk Factors:
- Age: SPS typically affects people over the age of 60
- Family history: Having a family history of neurodegenerative diseases may increase the risk of developing SPS
- Genetics: Certain genetic mutations have been linked to an increased risk of developing SPS
Symptoms
The symptoms of SPS can vary from person to person, but common symptoms include:
- Difficulty moving the eyes, particularly in the vertical direction
- Problems with balance and walking, including frequent falls
- Muscle stiffness and rigidity
- Tremors
- Speech difficulties
- Swallowing problems
- Cognitive impairment, including memory loss and difficulty with concentration
Diagnosis
Diagnosing SPS can be challenging, as the symptoms are similar to those of other neurodegenerative diseases, such as Parkinson's disease. A diagnosis is typically made based on a combination of:
- Medical history and physical examination
- Imaging tests, such as MRI or CT scans, to rule out other conditions
- Lab tests, such as blood work and cerebrospinal fluid analysis
Treatment and Management
There is currently no cure for SPS, but treatment can help manage the symptoms. Treatment options may include:
- Medications to control muscle stiffness, tremors, and other motor symptoms
- Physical therapy to improve mobility and balance
- Occupational therapy to develop strategies for daily living
- Speech therapy to address communication difficulties
- Cognitive training to help manage cognitive impairment
Prognosis
The prognosis for SPS is generally poor, with most people experiencing significant disability within 5-7 years of symptom onset. However, with proper treatment and management, it is possible to slow the progression of the disease and improve quality of life.
Article last updated on: 18th June 2025.
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