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  • noun

Synonyms for CJD

rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus

References in periodicals archive ?
Les conditions d'eligibilite pour les jeunes dirigeants desirant participer au CJD Business Awards sont les suivantes :
MRI brain showed subtle increased signal in bilateral caudate nucleus and subcortical ribboning on DWI (Figure-1), suggestive of CJD.
Genetic screening and predicative pre--natal tests are available for familial CJD (Ryan, R.
And "if evidence to support a diagnosis of viral encephalitis, paraneoplastic disorder, depression, peripheral vertigo, Alzheimer's disease, stroke, dementia (nonspecified), CNS vasculitis, peripheral neuropathy, or Hashimoto encephalopathy is lacking, then the clinician should think about requesting an MRI with diffusion-weighted imaging/apparent diffusion coefficient sequences to look for changes associated with sporadic CJD," they suggested.
Magee said the city resident who died had classic CJD, not mad cow disease, which is much rarer.
Because CJD presentation varies widely, most clinicians will not consider the diagnosis until the disease has progressed or the patient has died.
Daughter Elizabeth added: "Because CJD is so rare, we felt like we had no-one to turn to.
More recently, in New Zealand, CJD has again come into the public eye with extensive media coverage (3).
Since 1996, in Japan, a nongovernmental CJD surveillance group supported by the Ministry of Health and Welfare (later renamed the Ministry of Health, Labour, and Welfare) has conducted a national survey seeking cases of human prion disease.
Prof James Ironside, of the National CJD Surveillance Unit at Edinburgh University, will tell an audience today that this underlines the need for a rapid screening test for the disease.
This is the first demonstration of a brain abnormality in healthy mutation carriers of CJD," said Dr.
So it is with the ongoing research into transmissible spongiform encephalopathy (TSE), a family of deadly neurological diseases, the most infamous of which are CJD (Creutzfeldt-Jakob disease) in humans and BSE in cattle.
The relative risk (RR) of CJD for CWD-endemic county residents was not significantly increased (RR 0.
The health ministry plans to provide 250,000 yen to subsidize each autopsy of a person suspected to have died from sporadic Creutzfeldt-Jakob disease to confirm whether they died from that or variant CJD, which is linked to mad cow disease, ministry officials said Saturday.
CJD, which strikes one in one million people, is also known as spongiform encephalopathy, and one form, bovine spongiform encephalopathy (also known as mad cow disease), can be transmitted to humans who have eaten contaminated beef.