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Creutzfeldt-Jakob disease

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Description

Prion disease represents a group of conditions that affect the nervous system in humans and animals. In people, these conditions impair brain function, causing changes in memory, personality, and behavior; a decline in intellectual function (dementia); and abnormal movements, particularly difficulty with coordinating movements (ataxia). The signs and symptoms of prion disease typically begin in adulthood and worsen with time, leading to death within a few months to several years.

MedlinePlus Genetics

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

0

Genes

External Links

  • OMIM

    123400

  • Orphanet
  • HPO
  • Medgen

    C0022336

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