Prion

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Prion
File:PDB 6DU9.png
Synonyms	N/A
Pronounce	N/A
Specialty	N/A
Symptoms	Dementia, ataxia, myoclonus, insomnia
Complications	Neurodegeneration, death
Onset	Varies, often in adulthood
Duration	Progressive
Types	N/A
Causes	Misfolded prion protein
Risks	Genetic predisposition, consumption of infected tissue
Diagnosis	Biopsy, MRI, EEG, CSF analysis
Differential diagnosis	Alzheimer's disease, Parkinson's disease, Huntington's disease
Prevention	N/A
Treatment	Supportive care
Medication	N/A
Prognosis	Poor
Frequency	Rare
Deaths	N/A

Prion disease is a group of rare, fatal neurodegenerative disorders caused by abnormally folded prion proteins that accumulate in the brain and lead to the destruction of nerve cells. Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), can affect both humans and animals. Examples of human prion diseases include Creutzfeldt-Jakob disease (CJD), variant Creutzfeldt-Jakob disease (vCJD), kuru, fatal familial insomnia (FFI), and Gerstmann-Sträussler-Scheinker syndrome (GSS).

File:Prion propagation.svg

Prion propagation

Signs and symptoms

The symptoms of prion disease can vary depending on the specific type of disease, but common signs and symptoms include:

• Rapidly progressive dementia
• Muscle stiffness or twitching
• Weakness and coordination problems
• Difficulty speaking or swallowing
• Behavioral changes, such as anxiety, depression, or irritability
• Sleep disturbances

As the disease progresses, severe disability and ultimately death typically occur.

Causes

Prion diseases are caused by misfolded prion proteins, which can induce normal proteins in the brain to adopt the abnormal shape, leading to the accumulation of these toxic proteins and the destruction of nerve cells. Prion diseases can be classified into three categories based on their mode of transmission:

• Sporadic: The most common form, which occurs spontaneously without any known cause
• Inherited: Caused by mutations in the PRNP gene, which is responsible for producing the normal prion protein
• Acquired: Resulting from exposure to contaminated brain or nervous system tissue, either through direct contact or consumption of infected material

Risk factors

Risk factors for developing prion disease include:

• Family history of prion disease, particularly for inherited forms
• Exposure to contaminated brain or nervous system tissue, either through medical procedures or contact with infected individuals
• Consumption of contaminated meat, as seen in variant CJD, which is linked to the consumption of beef products contaminated with bovine spongiform encephalopathy (BSE) or "mad cow disease"

Diagnosis

Diagnosing prion disease can be challenging, as its symptoms can mimic those of other neurodegenerative disorders. A clinical examination, including a detailed medical history and assessment of symptoms, is typically the first step in the diagnostic process. Additional tests that may be performed include:

• Brain imaging, such as magnetic resonance imaging (MRI) or computed tomography (CT) scans, to detect changes in brain structure
• Electroencephalogram (EEG) to monitor brain activity
• Cerebrospinal fluid tests to check for the presence of specific biomarkers indicative of prion disease
• Genetic testing for inherited forms of prion disease

In rare cases, a brain biopsy may be performed to confirm the diagnosis, but this is generally avoided due to the risk of transmitting the disease during the procedure.

Treatment

There is currently no cure for prion disease, and no specific antiprion medications are available. Treatment focuses on providing supportive care and managing symptoms to improve the quality of life for affected individuals. This may include:

• Medications to manage pain, muscle stiffness, or other symptoms
• Physical, occupational, and speech therapy to help maintain function and improve quality of life
• Nutritional support, including the use of feeding tubes if swallowing becomes difficult
• Emotional support and counseling for both affected individuals and their families

Prevention

While there is no guaranteed way to prevent prion disease, particularly for sporadic cases, certain precautions can be taken to reduce the risk of transmission:

• Proper sterilization of surgical instruments and adherence to infection control measures in healthcare settings
• Reporting and monitoring of animal prion diseases, such as BSE, to prevent contamination of the food supply
• Avoiding the consumption of brain and nervous system tissue from animals, particularly in regions where prion diseases are known to occur
• Genetic counseling and testing for individuals with a family history of inherited prion disease

See also

• Creutzfeldt-Jakob disease (CJD)
• Variant Creutzfeldt-Jakob disease (vCJD)
• Kuru
• Fatal familial insomnia (FFI)
• Gerstmann-Sträussler-Scheinker syndrome (GSS)
• Bovine spongiform encephalopathy (BSE)

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