Creutzfeldt-Jakob disease

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Related to Creutzfeldt-Jakob disease: Huntington's disease, mad cow disease

Creutzfeldt-Jakob disease:

see prionprion
, abnormal form of a protein found in mammals, now generally believed to cause a group of diseases known as prion diseases or transmissible spongiform encephalopathies, which are rare progressive degenerative neurological disorders.
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References in periodicals archive ?

In March of 1996, scientists reported that ten people in Great Britain had been diagnosed with a new form of Creutzfeldt-Jakob Disease called V-CJD ("V" for "variant").

Mad about BSE

Britain recorded the world's first case of vCJD (variant Creutzfeldt-Jakob disease) infection by blood transfusion in 2004.

British Vegetarian Ritchii Kara Diagnosed with Mad Cow Disease

Creutzfeldt-Jakob disease (CJD) is a progressive neurological disorder that affects only about 1 in a million people each year worldwide, according to the National Institutes of Health (NIH). There are about 350 cases in the U.S.

Man Contracts Rare Disorder After Eating Squirrel Brains

First symptom in sporadic Creutzfeldt-Jakob disease. Neurology.

Creutzfeldt Jakob disease masquerading as severe depression: a case report

The results are notable for abnormal restricted diffusion in the caudate and putamen bilaterally, which is consistent with Creutzfeldt-Jakob disease (CJD).

Sudden-onset memory problems, visual hallucinations, and odd behaviors

Keywords: Creutzfeldt-Jakob disease, cortical blindness, Heidenhain variant

Differential Diagnosis of Cortical Blindness, Creutzfeldt-Jakob Disease, Heidenhain Variant/Kortikal Korlugun Ayirici Tanisi, Creutzfeldt Jakob Hastaligi, Heidenhain Varyanti

Creutzfeldt-Jakob disease (CJD) is a fatal neurodegenerative disorder that, according to the most well-accepted hypothesis (1), is caused by replicating, transmissible, abnormal forms of a host-encoded prion protein (prions).

Update: Dura Mater Graft-Associated Creutzfeldt-Jakob Disease--Japan, 1975-2017

Beydoun, "Sporadic Creutzfeldt-Jakob disease presenting with nonconvulsive status epilepticus," Epilepsy & Behavior, vol.

Creutzfeldt-Jakob Disease Presenting as Expressive Aphasia and Nonconvulsive Status Epilepticus

Here, we describe the case of an elderly woman with sporadic Creutzfeldt-Jakob disease (sCJD) who, shortly after presentation of the initial symptoms of the disease, demonstrated a rapid deterioration of consciousness and EEG features suggestive of NCSE.

Creutzfeldt-Jakob Disease Presenting as Nonconvulsive Status Epilepticus

In the Introduction of the article titled "A Case of Sporadic Creutzfeldt-Jakob Disease Presenting as Conversion Disorder" [1], the text reading "Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, fatal neurodegenerative disease caused by aggregation of misfolded prion proteins.

Corrigendum to "A Case of Sporadic Creutzfeldt-Jakob Disease Presenting as Conversion Disorder"

EDINBURGH, U.K., November 20, 2017 -- Scientists here have developed a new system to study Creutzfeldt-Jakob disease in the lab, paving the way for research to find treatments for the fatal brain disorder.

New Way To Study Brain Disease Uses Neuro-Cells From Stem Cells

To the Editor: The recent etymologia article on Creutzfeldt-Jakob disease by Henry and Murphy (1) does not accurately reflect current understanding of the contributions of Creutzfeldt and Jakob.