Creutzfeldt-Jakob Disease
'New CJD type' discovered in US
A new form of Creutzfeldt-Jakob Disease (CJD) may have been uncovered in a handful of patients in the US.
Ref. https://news.bbc.co.uk/1/hi/health/7497867.stm
Creutzfeldt-Jakob Disease
This genetic disorders:** known as Creutzfeldt-Jakob Disease, can be Discussed here.
Persons finding themselves or loved ones socially unsettling because of Creutzfeldt-Jakob disease, related: prion disease may like to share how they cope in order to help others world-wide searching for experiences.
** A mutation / chromosome / missing or additional gene(s)
Rare case of brain disease
An Auckland patient is the latest person to be diagnosed with the incurable brain disorder Creutzfeldt-Jakob disease (CJD), a condition that became notorious because of its association with Britain's "Mad cow disease" Outbreak of the mid-1990s. Ref. Source 6
Toxic byproduct of hemoglobin could provide clues for cerebral hemorrhage and Creutzfeldt-Jakob Disease
A novel mechanism has been found that could protect the brain from damage due to stroke and a variety of neurodegenerative conditions, including sporadic Creutzfeldt-Jakob disease, Alzheimer’s disease, and Parkinson’s disease, report scientists. Ref. Source 1p.
Prion protein found in skin of CJD patients. Scientists have detected abnormal prion protein in the skin of several people who died from Creutzfeldt-Jakob disease (CJD). The scientists also exposed healthy mice to skin extracts from two CJD patients, and all developed prion disease. The study results raise questions about the possible transmissibility of prion diseases via medical procedures involving skin, and whether skin samples might be used to detect prion disease. Source 5w.
New skin test detects prion infection before symptoms appear. Prions can infect both humans and animals, causing Creutzfeldt-Jakob disease (CJD) in humans, mad cow disease in cattle, and chronic wasting disease in elk and deer. The infectious, misfolded protein particles often go undetected as they destroy brain tissue, causing memory loss, mobility issues, and ultimately death. Preclinical detection of prions has proven difficult, but new research suggests skin samples hold early signs of prion disease that precede neurologic symptoms. Source 2k.