creutzfeldt-jakob disease Antonyms

No Synonyms and anytonyms found

Meaning of creutzfeldt-jakob disease

Wordnet

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

  1. Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disorder.
  2. There are different types of Creutzfeldt-Jakob disease, including sporadic, familial, and acquired forms.
  3. The symptoms of Creutzfeldt-Jakob disease typically include rapidly progressive dementia, involuntary movements, and muscle stiffness.
  4. Creutzfeldt-Jakob disease is caused by abnormal proteins called prions that affect the brain's function.
  5. The diagnosis of Creutzfeldt-Jakob disease often relies on clinical symptoms, brain imaging, and cerebrospinal fluid analysis.
  6. Unfortunately, there is currently no cure for Creutzfeldt-Jakob disease, and treatment focuses on managing symptoms and providing supportive care.
  7. 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."
  8. Creutzfeldt-Jakob disease is not contagious through casual contact, but precautions are necessary when handling brain tissue or contaminated surgical instruments.
  9. The prevalence of Creutzfeldt-Jakob disease is low, with only a few hundred cases reported worldwide each year.
  10. 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.