Chronic debilitating disease is a highly contagious fatal neurodegenerative disease affecting the cervix in North America (Belay et al., 2004; Saunders et al., 2012). It is known that only four types of cervicitis, including elk, moose, white tailed, and moose, are suffering from this disease (chronic consumption type disease alliance). It is classified as infectious spongiform encephalopathy (TSE) also known as prion disease (Belay et al., 2004). Prions are irregular virulence factors that cause abnormal folding of specific proteins called prions.
Chronic wasting disease transmitted by misfolded protein known as prion affects elk brain tissue and has been detected across North America. Moose, originally recorded in the late 1960s, affected elk of the game farm and wildlife in many areas. This disease elk begins experiencing weight loss, increased drinking demand, disorientation disorder, and inconspicuousness, and disease develops to death at the stage of progression. This disease is similar to mad cow disease, but it is not identical, it does not document the danger to humans, it does not prove that this disease poses a threat to livestock. In 2002, due to fear of chronically wasteful diseases, Korea banned imports of elk's horns
Some Michigan seemingly sporadic young men cases may refer to chronic wasting disease (CWD) from deer or elk, that is, a hunter who is infected with animal prion diseases. CWD is becoming more common in US animal populations. Since hunters eat meat of these animals, prion diseases may proceed from hunters to hunters. Another form of human prion disease is called Kuru disease. They discovered ceremonial cannibalism among the indigenous peoples of New Guinea (especially they eat humans and their brains). When people with sporadic CJD are eaten, sickness may begin. After the symptoms appear, death of about comes about 1 year, but the average incubation period is about 12 years, it will be 40 years. At the end of these ceremonies, this disease almost disappeared in New Guinea.