Creutzfeldt Jakob Disease (CJD)

Creutzfeldt-Jakob disease is a rare and fast-developing condition that damages brain cells, leading to rapid mental decline and physical symptoms like muscle stiffness and difficulty walking.

What is Creutzfeldt-Jakob disease?

Creutzfeldt-Jakob disease (CJD) is a rare, progressive brain disorder that affects how people think and behave. It can cause serious problems with memory, coordination, and movement.

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What are the symptoms of Creutzfeldt-Jakob disease?

People with Creutzfeldt-Jakob disease may experience a range of symptoms, including:

  • Memory problems
  • Changes in personality or mood
  • Difficulty walking or maintaining balance
  • Blurred or double vision
  • Muscle stiffness or jerky movements
  • seizures

What causes Creutzfeldt-Jakob disease?

The exact cause of Creutzfeldt-Jakob disease is not fully understood. However, it is linked to abnormal proteins called prions that can damage brain tissue. In most cases, it appears without any known reason, but some forms can be inherited.

How common is Creutzfeldt-Jakob disease?

Creutzfeldt-Jakob disease is very rare. It affects about one person in every million each year in the UK, making it an uncommon condition.

Who is more likely to get Creutzfeldt-Jakob disease?

A few factors can increase the chance of getting Creutzfeldt-Jakob disease, including:

  • People in their 60s and older are more affected
  • Rare genetic forms can run in families

Final thoughts

Creutzfeldt-Jakob disease is a serious condition that affects how people think and move. If you or someone you know is experiencing symptoms, it’s important to speak to your GP or healthcare provider for guidance.

Always consult a medical professional
This article is for informational purposes only and is not a substitute for medical advice. Always consult a healthcare professional before starting, stopping or changing any medication. If you have concerns about your medication or experience side effects, speak to your doctor or pharmacist immediately.

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