Enfermedades Causadas por priones

Franco Romero Cinthya GuadalupeRomero Cordero Viridiana

¿Qué es un prion?

Priones y Prpc

Prpc y PrPSc

¿Cómo las PrPsc atacan al cerebro?

Deterioro Neuronal

Infección en animales y humanos

Enfermedades causadas por priones

Kuru

Creutzfeldt-Jakob

Insomniofamiliar

fatal

BibliografíaPatrick R. Murray, Ken S. Rosenthal y Michael A. Pfaller. Microbiología médica. 6ª ed. ELSEVIER, 2011, p.661.

Martinez, C. (2006, septiembre). Fisiopatología de las enfermedades por priones. México: Gaceta Medica.

Ryan R, Hill S, Lowe D, Allen K, Taylor M, Mead C. Notification and support for people exposed to the risk of Creutzfeldt Jakob disease (CJD) (or other prion diseases) through medical treatment ‐(iatrogenically). Cochrane Database of Systematic Reviews 2011, Issue 3. Art. No.: CD007578. DOI: 10.1002/14651858.CD007578.pub2.

Stewart LA, Rydzewska LH, Keogh GF, Knight RS. Systematic review of therapeutic interventions in human prion disease. Neurology 2008; 70(15): 1272-1281.

Prion disease blood test using immunoprecipitation and improved quaking-induced conversion. Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA. MEDLINE. Mayo 2011. PMID: 21558432

Prusiner Stanley. Prions. Gran Bretaña. Vol. 95 No. 23. 2009.Belay E. “Transmissible Spongiform Encelophalopathies in Humans”.Atlanta, Georgia, UnitedStates. Annue. Rev. Microbiol. 2011.53:283-214.2001.

Belay. E. “ The Public Healt Impact of Pion Diseases”. Atlanta, Georgia, United States. Annu. Rev. Public Health. 2005.26.191-212. 2005