Sporadic Creutzfeldt-Jakob disease with unusual initial presentation as posterior reversible encephalopathy syndrome: a case report

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Dirzius, Edgaras; Balnyte, Renata; Steibliene, Vesta; Gleizniene, Rymante; Gudinaviciene, Inga; Radziunas, Andrius; Petrikonis, Kestutis;
(2016)

Background Creutzfeldt - Jakob disease (CJD) is a rapidly progressive and fatal neurodegenerative prion disease. MRI findings are included in diagnostic criteria for probable CJD, giving a sensitivity and specificity more than 90%, but the atypical radiological presenta... View more
  • References (41)
    41 references, page 1 of 5

    1. Geschwind MD. Prion diseases. Continuum (Minneap. Minn). [Internet], vol. 21. 2015. p. 1612-38. NIH Public Access. Available from: http://www.ncbi. nlm.nih.gov/pubmed/26633779. [cited 2016 Jul 6].

    2. Prusiner SB. Prions. Proc Natl Acad Sci U S A. 1998;95:13363-83.

    3. Chen C, Dong X-P. Epidemiological characteristics of human prion diseases. Infect Dis Poverty [Internet]. 2016;5:47. BioMed Central. Available from: http://idpjournal.biomedcentral.com/articles/10.1186/s40249-016-0143-8. [cited 2016 Jun 24].

    4. Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P, et al. Sporadic human prion diseases: molecular insights and diagnosis. Lancet Neurol [Internet]. 2012;11:618-28. Elsevier. Available from: http://www.ncbi.nlm.nih. gov/pubmed/22710755. [cited 2016 Jul 6].

    5. Brown P, Gibbs CJ, Rodgers-Johnson P, Asher DM, Sulima MP, Bacote A, et al. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol [Internet]. 1994;35:513-29. Available from: http://www.ncbi.nlm.nih.gov/ pubmed/8179297. [cited 2015 Jul 12].

    6. Kretzschmar HA. Human prion diseases (spongiform encephalopathies). Arch Virol Suppl [Internet]. 1993;7:261-93. Available from: http://www.ncbi. nlm.nih.gov/pubmed/8219808. [cited 2016 Jul 6].

    7. Kurian M a, Li Y, Zhen J, Meyer E, Hai N, Jardine P, et al. Lancet Neurology. Lancet Neurol. 2010.

    8. Skinningsrud A, Stenset V, Gundersen AS, Fladby T. Cerebrospinal fluid markers in Creutzfeldt-Jakob disease. Cerebrospinal Fluid Res [Internet]. 2008;5:14. Available from: http://www.pubmedcentral.nih.gov/ articlerender.fcgi?artid=2531166&tool=pmcentrez&rendertype=abstract. [cited 2015 Aug 9].

    9. Wieser HG, Schwarz U, Blättler T, Bernoulli C, Sitzler M, Stoeck K, et al. Serial EEG findings in sporadic and iatrogenic Creutzfeldt-Jakob disease. Clin Neurophysiol [Internet]. 2004;115:2467-78. Elsevier. Available from: http:// linkinghub.elsevier.com/retrieve/pii/S1388245704002123. [cited 2016 Jul 6].

    10. Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain [Internet]. 2009;132:2659-68. Oxford University Press. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19773352. [cited 2016 Jul 6].

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