Understanding Creutzfeldt-Jakob Disease (CJD) By: Nichole Michael-Avabore
Introduction Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, and always fatal neurodegenerative disorder. It belongs to a family of diseases known as prion diseases, also called Transmissible Spongiform Encephalopathies (TSEs). Spongiform refers to the way affected brains look. With prion diseases, the brain is filled with holes and looks like a sponge when the tissue is examined under a microscope. Like other prion diseases, CJD causes problems with muscle coordination, thinking, and memory. There are about 350 cases per year in the United States, and about 70% of people with CJD die within one year of getting the disease. Why Is It Important? It is vital to understand CJD because it is rare, and although it isn’t very well known, it is universally fatal. Many people struggle with dementia, problems with thinking, balance problems, etc. As of now, there is no known cure; thus, research is vital for developing early diagnostic tests and effective treatments. Who It Affe...