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dc.contributor.authorBancalari-Benavides, E.
dc.contributor.authorRodriguez-Calienes, A.
dc.contributor.authorCamacho-Caballero, K.
dc.date.accessioned2025-10-31T18:33:07Z
dc.date.available2025-10-31T18:33:07Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/20.500.12805/4866
dc.description.abstractCreutzfeldt-Jakob disease (CJD) is the commonest human prion disease with a reported annual incidence rate of one per million worldwide. CJD has a bad prognosis, and the mean length of survival is 4-6 months. Only 11 cases have been reported in the literature from Peru. Thus, we report a case of a 66-year-old male patient with the diagnosis of probable sporadic CJD in whom the survival duration was of 25 months. We identify that the time from disease onset to myoclonus and to reach the akinetic mutism state, the absence of early imaging findings, the delayed cortical and basal ganglia involvement and the supportive therapies implemented were factors that could contribute for the long survival in this patient.en_US
dc.formatapplication/pdf
dc.language.isospa
dc.publisherFacultad de Medicina, Universidad Nacional Mayor de San Marcos
dc.relation.ispartofurn:issn:1609-9419
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectPrion Proteins and Amyloid Aggregation in Diseaseen_US
dc.subjectPrion Diseases and Their Diagnostic Innovationsen_US
dc.titleUn caso probable de enfermedad de Creutzfeldt-Jacob de variante esporádica con larga supervivencia en Perúes_PE
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.15381/anales.v82i1.19545
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.25
dc.type.otherResearch article
dc.identifier.journalAnales de la Facultad de Medicina
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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