Creutzfeldt-Jakob disease causes: Difference between revisions
Line 5: | Line 5: | ||
==Causes== | ==Causes== | ||
[[Transmissible spongiform encephalopathy]] diseases are caused by [[prion]]s. The diseases are thus sometimes called prion diseases. Other prion diseases include [[Gerstmann-Sträussler-Scheinker syndrome]] (GSS), [[fatal familial insomnia]] (FFI) and [[kuru (disease)|kuru]] in humans, as well as [[bovine spongiform encephalopathy]] (BSE) commonly known as mad cow disease, [[chronic wasting disease]] (CWD) in elk and deer, and [[scrapie]] in sheep. | [[Transmissible spongiform encephalopathy]] diseases are caused by [[prion]]s. The diseases are thus sometimes called prion diseases. Other prion diseases include [[Gerstmann-Sträussler-Scheinker syndrome]] (GSS), [[fatal familial insomnia]] (FFI) and [[kuru (disease)|kuru]] in humans, as well as [[bovine spongiform encephalopathy]] (BSE) commonly known as mad cow disease, [[chronic wasting disease]] (CWD) in elk and deer, and [[scrapie]] in sheep. The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable [[chemical conformation|conformations]]. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates. | ||
The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable [[chemical conformation|conformations]]. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates | |||
==References== | ==References== |
Revision as of 18:39, 26 December 2012
Creutzfeldt-Jakob disease Microchapters |
Differentiating Creutzfeldt-Jakob disease from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Creutzfeldt-Jakob disease causes On the Web |
American Roentgen Ray Society Images of Creutzfeldt-Jakob disease causes |
Risk calculators and risk factors for Creutzfeldt-Jakob disease causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Causes
Transmissible spongiform encephalopathy diseases are caused by prions. The diseases are thus sometimes called prion diseases. Other prion diseases include Gerstmann-Sträussler-Scheinker syndrome (GSS), fatal familial insomnia (FFI) and kuru in humans, as well as bovine spongiform encephalopathy (BSE) commonly known as mad cow disease, chronic wasting disease (CWD) in elk and deer, and scrapie in sheep. The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable conformations. One, the native state, is water-soluble and present in healthy cells. As of 2006, its biological function is unknown. The other conformational state is very poorly water-soluble and readily forms protein aggregates.