Prion Diseases.

Abstract:

:Prions diseases are uniformly fatal neurodegenerative diseases that occur in sporadic, genetic, and acquired forms. Acquired prion diseases, caused by infectious transmission, are least common. Most prion diseases are not infectious, but occur spontaneously through misfolding of normal prion proteins or genetic mutations in the prion protein gene. Although most prion diseases are not caused by infection, they can be transmitted accidentally. Certain infection control protocols should be applied when handling central nervous system and other high-risk tissues. New diagnostic methods are improving premortem and earlier diagnosis. Treatment trials have not shown improved survival, but therapies may be available soon.

journal_name

Neurol Clin

journal_title

Neurologic clinics

authors

Tee BL,Longoria Ibarrola EM,Geschwind MD

doi

10.1016/j.ncl.2018.07.005

subject

Has Abstract

pub_date

2018-11-01 00:00:00

pages

865-897

issue

4

eissn

0733-8619

issn

1557-9875

pii

S0733-8619(18)31248-9

journal_volume

36

pub_type

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