creutzfeldt-jakob disease Synonyms
No Synonyms and anytonyms found
creutzfeldt-jakob disease Meaning
creutzfeldt-jakob disease (n)
rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus; characterized by progressive dementia and gradual loss of muscle control
creutzfeldt-jakob disease Sentence Examples
- Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disorder.
- There are different types of Creutzfeldt-Jakob disease, including sporadic, familial, and acquired forms.
- The symptoms of Creutzfeldt-Jakob disease typically include rapidly progressive dementia, involuntary movements, and muscle stiffness.
- Creutzfeldt-Jakob disease is caused by abnormal proteins called prions that affect the brain's function.
- The diagnosis of Creutzfeldt-Jakob disease often relies on clinical symptoms, brain imaging, and cerebrospinal fluid analysis.
- Unfortunately, there is currently no cure for Creutzfeldt-Jakob disease, and treatment focuses on managing symptoms and providing supportive care.
- Variant Creutzfeldt-Jakob disease (vCJD) gained attention in the late 20th century due to its link to bovine spongiform encephalopathy (BSE), or "mad cow disease."
- Creutzfeldt-Jakob disease is not contagious through casual contact, but precautions are necessary when handling brain tissue or contaminated surgical instruments.
- The prevalence of Creutzfeldt-Jakob disease is low, with only a few hundred cases reported worldwide each year.
- Research into Creutzfeldt-Jakob disease continues in hopes of better understanding its mechanisms and developing effective treatments.
FAQs About the word creutzfeldt-jakob disease
rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus; characterized by progressive dementia and gradual loss of muscl
No synonyms found.
No antonyms found.
Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disorder.
There are different types of Creutzfeldt-Jakob disease, including sporadic, familial, and acquired forms.
The symptoms of Creutzfeldt-Jakob disease typically include rapidly progressive dementia, involuntary movements, and muscle stiffness.
Creutzfeldt-Jakob disease is caused by abnormal proteins called prions that affect the brain's function.