Creutzfeldt-Jakob disease

CJD (Creutzfeldt Jakob disease)|Creutzfeldt Jacob syndrome|Creutzfeldt Jakob disease|Creutzfeldt-Jacob disease|Jakob-Creutzfeldt disease|Subacute spongiform encephalopathy|Transmissible virus dementia (disorder)|Transmissible virus dementia|Classic Creutzfeldt-Jakob Disease|Creutzfeldt-Jakob Disease

Creutzfeldt???Jakob_disease

degenerative neurological disorder

Spongiform degeneration in Creutzfeldt-Jakob disease.jpg

Degenerative neurological disorder

<span lang="en" dir="ltr"><span class="mw-page-title-main">Creutzfeldt???Jakob disease</span></span>

Creutzfeldt???Jakob disease (CJD) is an incurable, always fatal, neurodegenerative disease belonging to the transmissible spongiform encephalopathy (TSE) group. Early symptoms include memory problems, behavioral changes, poor coordination, visual disturbances and auditory disturbances. Later symptoms include dementia, involuntary movements, blindness, deafness, weakness, and coma. About 70% of sufferers die within a year of diagnosis. The name "Creutzfeldt???Jakob disease" was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.

en

https://upload.wikimedia.org/wikipedia/commons/b/bb/Practneurol-2016-001571f02.jpg

1356778954

https://upload.wikimedia.org/wikipedia/commons/thumb/b/bb/Practneurol-2016-001571f02.jpg/330px-Practneurol-2016-001571f02.jpg

Creutzfeldt???Jakob disease

standard