{"id":12920,"date":"2024-08-23T08:15:31","date_gmt":"2024-08-23T06:15:31","guid":{"rendered":"https:\/\/valintermed.com\/?p=12920"},"modified":"2024-08-23T08:15:31","modified_gmt":"2024-08-23T06:15:31","slug":"podostryy-skleroziruyuschiy-panentsefalit","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/subacute-sclerotic-pancreatitis\/","title":{"rendered":"Subacute sclerosing panencephalitis"},"content":{"rendered":"
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Subacute sclerosing panencephalitis (SSPE) is a progressive disease of the central nervous system that usually occurs against the background of a previous measles infection. It is characterized by a long and slow development of neurological symptoms, such as changes in behavior, cognitive impairment, seizures, and loss of movement. The pathology is caused by an infection with the measles virus, which leads to irreversible changes in neuronal cells and brain structure. Diagnosis of the disease is often based on clinical manifestations, anamnesis, and imaging methods, as well as laboratory tests aimed at detecting antibodies to the measles virus. Studying this disease is important, as it poses a threat to the health of children and young people, allowing us to better understand the mechanisms of inflammatory and degenerative processes in the neurosystem.<\/p>\n

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