Creutzfeldt-Jakob disease natural history, complications and prognosis: Difference between revisions
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{{Creutzfeldt-Jakob disease}} | {{Creutzfeldt-Jakob disease}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
Creutzfeldt Jakob disease is rapidly progressive and always fatal. | Once symptoms develop, Creutzfeldt-Jakob disease is rapidly progressive and almost always fatal. Early symptoms are often non-specific. Patients' relatives usually report rapidly progressive dementia, personality changes, and sleep disorders. The majority of patients (85% of patients) die within 1 year of symptom-onset. Common complications of Creutzfeldt-Jakob disease include overwhelming infections, congestive heart failure, or respiratory failure. | ||
==Natural History== | |||
*Once symptoms develop, Creutzfeldt-Jakob disease is rapidly progressive and almost always fatal. | |||
*Early symptoms are often non-specific. Patients' relatives usually report rapidly progressive dementia, personality changes, and sleep disorders. | |||
*The majority of patients (85% of patients) die within 1 year of symptom-onset, often due to complicatioons succh as overwhelming infections, congestive heart failure, or respiratory failure.<ref name="www.cdc.gov">{{Cite web | last = | first = | title = http://www.cdc.gov/ncidod/dvrd/cjd/index.htm | url = http://www.cdc.gov/ncidod/dvrd/cjd/index.htm | publisher = | date = | accessdate = 17 February 2014 }}</ref> | |||
==Complications== | ==Complications== | ||
Complications of Creutzfeldt-Jakob disease include the following: | |||
* [[Infection]] | * [[Infection]] | ||
* [[ | * [[Heart failure]] | ||
* [[Respiratory failure]] | * [[Respiratory failure]] | ||
* Death | * Death | ||
==Prognosis== | ==Prognosis== | ||
* The | *The prognosis of Creutzfeldt-Jakob disease is very poor. | ||
*Patients usually die within 6 to 12 months of symptom-onset. | |||
* | * A few reports described individuals surviving beyond than 1 or 2 years after diagnosis. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
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{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Infectious disease]] | [[Category:Infectious disease]] | ||
[[Category:Neurology]] | [[Category:Neurology]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Transmissible spongiform encephalopathies]] | [[Category:Transmissible spongiform encephalopathies]] | ||
Revision as of 20:30, 17 March 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Once symptoms develop, Creutzfeldt-Jakob disease is rapidly progressive and almost always fatal. Early symptoms are often non-specific. Patients' relatives usually report rapidly progressive dementia, personality changes, and sleep disorders. The majority of patients (85% of patients) die within 1 year of symptom-onset. Common complications of Creutzfeldt-Jakob disease include overwhelming infections, congestive heart failure, or respiratory failure.
Natural History
- Once symptoms develop, Creutzfeldt-Jakob disease is rapidly progressive and almost always fatal.
- Early symptoms are often non-specific. Patients' relatives usually report rapidly progressive dementia, personality changes, and sleep disorders.
- The majority of patients (85% of patients) die within 1 year of symptom-onset, often due to complicatioons succh as overwhelming infections, congestive heart failure, or respiratory failure.[1]
Complications
Complications of Creutzfeldt-Jakob disease include the following:
Prognosis
- The prognosis of Creutzfeldt-Jakob disease is very poor.
- Patients usually die within 6 to 12 months of symptom-onset.
- A few reports described individuals surviving beyond than 1 or 2 years after diagnosis.
References
- ↑ "http://www.cdc.gov/ncidod/dvrd/cjd/index.htm". Retrieved 17 February 2014. External link in
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