Changes

Transmissible Spongiform Encephalopathies (TSEs) are neurological diseases that have been found in humans, cattle, sheep and other mammals (e.g. cats, goats, deer, antelope). The agent of disease is believed to be an abnormal prion protein (or is prion associated). An abnormal prion is a protein with an abnormal folding structure when compared to the naturally occurring prion found in nervous and lymphoreticular tissues. Various abbreviations are in use to refer to this: Prion Protein (PrP); Abnormal Prion Protein (PrP^ab); Resistant Prion Protein (PrP^res); Scrapie Prion Protein PrP^sc) and others.

Transmissible Spongiform Encephalopathies (TSEs) are neurological diseases that have been found in humans, cattle, sheep and other mammals (e.g. cats, goats, deer, antelope). The agent of disease is believed to be an abnormal prion protein (or is prion associated). An abnormal prion is a protein with an abnormal folding structure when compared to the naturally occurring prion found in nervous and lymphoreticular tissues. Various abbreviations are in use to refer to this: Prion Protein (PrP); Abnormal Prion Protein (PrP^ab); Resistant Prion Protein (PrP^res); Scrapie Prion Protein PrP^sc) and others.

==Signalment==

==Signalment==

==Clinical Signs==

==Clinical Signs==

Clinical signs include progressive ataxia and pruritus.

Clinical signs include progressive ataxia and pruritus.

==Treatment==

==Treatment==

==Control==

==Control==

==Refereneces==

==Refereneces==

 

[[Category:Transmissible_Spongiform_Encephalopathies]]

[[Category:Transmissible_Spongiform_Encephalopathies]]

[[Category:To_Do_-_Jaimie Meagor]]

[[Category:To_Do_-_Jaimie Meagor]]