Creutzfeldt-Jakob disease history and symptoms: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 4: | Line 4: | ||
{{Creutzfeldt-Jakob disease}} | {{Creutzfeldt-Jakob disease}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | |||
Creutzfeldt Jakob disease presents with rapidly progressive dementia and myoclonus.<ref name="Haywood-1997">{{Cite journal | last1 = Haywood | first1 = AM. | title = Transmissible spongiform encephalopathies. | journal = N Engl J Med | volume = 337 | issue = 25 | pages = 1821-8 | month = Dec | year = 1997 | doi = 10.1056/NEJM199712183372508 | PMID = 9400041 }}</ref> | |||
==History and Symptoms== | ==History and Symptoms== | ||
Revision as of 01:39, 17 February 2014
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
Creutzfeldt-Jakob disease Microchapters |
Differentiating Creutzfeldt-Jakob disease from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Creutzfeldt-Jakob disease history and symptoms On the Web |
American Roentgen Ray Society Images of Creutzfeldt-Jakob disease history and symptoms |
Risk calculators and risk factors for Creutzfeldt-Jakob disease history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Creutzfeldt Jakob disease presents with rapidly progressive dementia and myoclonus.[1]
History and Symptoms
The first symptom of CJD is rapidly progressive