Creutzfeldt-Jakob review based on two clinical cases in Hospital Universitario San Ignacio

Article Spanish OPEN
Pretelt, Felipe; Rivera, Neiby; Ursida, Valentina; Tovar, Catherin; Ramírez, Ayelet;
(2016)
  • Publisher: Asociación Colombiana de Neurología
  • Subject: rapidly progressive dementia | 14-3-3 protein | proteína 14-3-3 | prionopatía esporádica | DWI | proteína Tau | Creutzfeld-Jakob disease | diffusion weighted imaging | enfermedad de Creutzfeld-Jakob | demencia rápidamente progresiva | Tau protein | RMN DWI

La enfermedad de Creutzfeld-Jakob es una patología neurodegenerativa fatal e intratable, que hace parte de las denominadas encefalopatías espongiformes y se produce por la acumulación anormal de la PrP (proteína priónica patogénica),denominada PrPsc, a nivel del sistema... View more
  • References (10)

    1. RODRIGUEZ DR, CILLIANI B. Encefalopatías espongiformes transmisibles. Infectio. 2004;8:9.

    2. Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P. Sporadic human prion diseases: Molecular insights and diagnosis. Lancet Neurol. Elsevier Ltd; 2012;11(7):618-28.

    3. VAN EVERBROECK B, BOONS J, CRAS P. Cerebrospinal uflid biomarkers in Creutzfeldt-Jakob disease. Clin Neurol Neurosurg. 2005;107(5):355-60.

    4. BARASHI NS, VARGAS C, ZARCO LA. Enfermedades priónicas humanas. Univ Medica. 2013; 54(4):495-516

    5. FORNER SA, TAKADA LT. Comparing CSF biomarkers and brain MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease. Neurology Clinical practice 2015,116-125.

    6. COULTHART, MB, ANCES BM. Creutzfeldt-Jakob disease the search for definitive diagnostic tests continues. Neurology Clinical practice 2015, 99-101.

    7. SHINOHARA MN, HAMAGUCHI T. Serum tau protein as a marker for the diagnosis of Creutzfeldt-Jakob disease. J Neurol 2011 258, 1464-1468.

    8. ZANUSSO G, FIORINI M, FERRARI S, ET AL. Cerebrospinal Fluid Markers in Sporadic Creutzfeldt-Jakob Disease. International Journal of Molecular Sciences. 2011;12(9):6281- 6292.

    9. COULTHART MB, JANSEN GH, OLSEN E, ET AL. Diagnostic accuracy of cerebrospinal uflid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study. BMC Neurology. 2011;11:133. F

    10. KARCH A, HERMANN P, PONTO C ET AL. Cerebrospinal lfuid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease. Neurobiology of aging 2015,1964-1968.

  • Similar Research Results (4)
  • Metrics
Share - Bookmark