Creutzfeldt-Jakob Disease (CJD)
Creutzfeldt-Jakob Disease (CJD) is a rare and serious brain disorder caused by abnormal proteins called prions. These prions can trigger rapid degeneration of brain tissue, leading to severe symptoms like memory loss, personality changes, and difficulty moving or speaking. CJD can occur spontaneously, be inherited, or result from exposure to infected tissue, usually through medical procedures. The disease progresses quickly, and currently, there is no cure or effective treatment. Awareness of CJD is important, especially for healthcare providers, due to its potential transmission through certain medical practices.
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Creutzfeldt-Jakob disease (CJD) is a rare, degenerative brain disorder caused by abnormal proteins called prions. These prions lead to the rapid deterioration of brain tissue, resulting in severe neurological symptoms such as memory loss, changes in behavior, vision problems, and muscle stiffness. CJD can occur spontaneously, be inherited, or result from exposure to infected tissue. It is usually fatal within a year of onset, and there is currently no cure. Due to its serious nature, understanding CJD and its transmission methods is important for public health and awareness.