A preliminary diagnosis can be made on observation of the above clinical signs. The disease is characterized by accumulation of prion protein in the medulla oblongata (obex) region of the brain, as well as other tissues (lymph nodes, spleen, tonsils, etc.) and can be confirmed on post mortem by the presence of the following histological changes in the brain: bilateral symmetrical vacuolation in the grey matter of the brain, immunohistochemical demonstration of the accumulation of the disease specific PrP<sup>sc</sup>, gliosis and hypertrophy of astrocytes, neuronal degeneration and cerebral amyloidosis. | A preliminary diagnosis can be made on observation of the above clinical signs. The disease is characterized by accumulation of prion protein in the medulla oblongata (obex) region of the brain, as well as other tissues (lymph nodes, spleen, tonsils, etc.) and can be confirmed on post mortem by the presence of the following histological changes in the brain: bilateral symmetrical vacuolation in the grey matter of the brain, immunohistochemical demonstration of the accumulation of the disease specific PrP<sup>sc</sup>, gliosis and hypertrophy of astrocytes, neuronal degeneration and cerebral amyloidosis. |