Jakob-Creutzfeldt Disease

Jakob-Creutzfeld disease (also known as Jacobs-Lowry disease) is a chronic progressive degenerative disease of the central nervous system that manifests itself in the form of severe brain deformation, leading to various psychiatric disorders. The syndrome was first described in 1923 by the German neurologist Abel Jacob and his colleagues, and by the German neurologist Henry Creitzfeld in 1691. Until now, the exact etiology and pathogenesis of the disease are unclear.

The disease is a neurodegenerative disorder that typically affects older adults over 60 years of age. Symptoms may include personality changes, increased irritability, hallucinations, psychotic episodes, and other neuropsychiatric disorders. It can affect the ability to concentrate, express thoughts and emotions, as well as memory and thinking. The syndrome is caused by a congenital pathological change

JACOB-CREUTZFELDT DISEASE

Jakob-Creutzfeldt disease (JCD) is an acute demyelinating autoimmune demyelinating-hypergammaglobulinemic disease of the central nervous system, characterized by a short period of febrile agitation and subsequent progressive psychosis with dementia over 2-5 years. Usually seen in older men. The onset of the disease is characterized by a long period of fever lasting from several hours to 7-9 days, transient paresthesia, dizziness, headache,