Creutzfeldt–Jakob disease (CJD)

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 Creutzfeldt–Jakob disease (CJD) is a fatal neurological brain disorder which is caused by a mutation in the gene for the body’s normal prion protein. It is similar to other neudegenerative diseases such as Alzheimer's disease and Huntington disease, due to the unique changes in brain tissue caused by this prion mutation. As a result, patients with CJD suffer a wide range of symptoms such as memory loss, inability to fuction independently and even impairment of vision. They eventually lose the ability to communicate and move, which will result in infections that lead to death[1].

  1. National Institute of Neurological Disorders and Stroke What is Creutzfeldt-Jakob disease? 2018[cited 21/8/18] Available from :
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