While CJD is an inherited disease it can also be acquired through iatrogenic transmission, which is accidental exposure to CJD prion-contaminated material through a medical procedure using tainted human matter or surgical instruments.
Historically speaking, this disease got its name from the first founder, Hans Gerhard Creutzfeldt. He examined patients with symptoms related to brain degeneration, which lead to the naming of the disease. Afterward Alfons Maria Jakob found more information regarding the disease, and thus, the "Creutzfeldt Jakob Disease" name was born.
Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease.
mad cow disease is when cows get it. when the disease is passed on 2 humans, it's called the Creutzfeldt-Jakob Disease. so technically its the same thing, just in different species
Human Prion DiseasesCreutzfeldt-Jakob Disease (CJD) Variant Creutzfeldt-Jakob Disease (vCJD)Gerstmann-Straussler-Scheinker SyndromeFatal Familial InsomniaKuru
CJD is a chronic progressive neurologic disease that is 100% fatal.
Seemed like you answered your own question. A man named Jakob Creutzfeld was infected with it in the mid-19th century, thus naming the disease after him. FACT: Creutzfeld-Jakobs disease is 80% fatal. Go see a doctor!
If you are talking about the Kuru Disease, the scientific name is Creutzfeldt-Jakob.
Prions are abnormal, infectious proteins that can be acquired through consumption of contaminated meat or exposure to infected brain or nervous tissue. They can lead to degenerative brain diseases such as Creutzfeldt-Jakob disease in humans.
CJD typically occurs between the ages of 50 and 75.
Prion
Spongiform encephalopathies are thought to be caused by abnormal prion proteins that trigger a cascade of events leading to neuronal death, resulting in sponge-like holes in the brain tissue. These diseases include Creutzfeldt-Jakob disease, variant Creutzfeldt-Jakob disease, and bovine spongiform encephalopathy (mad cow disease).