Prion disease: Review of the literature.

Prion disease are entities of unknown genetic origin that cause in human beings a number of neurological manifestations that lead patients to states of immobility and severe deterioration, with a very poor prognosis and uncertain cure rates. It is difficult to find in the literature important findin...

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Fecha de publicación:: 2022

Institución:: Pontificia Universidad Javeriana Cali

Repositorio:: Vitela

Idioma:: spa

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network_acronym_str	Vitela2
network_name_str	Vitela
repository_id_str
spelling	Hernández, JonattanZaninovich-Ruiz, MilizaValencia, Henry2022-04-302023-10-11T04:35:10Z2023-10-11T04:35:10Zhttps://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/695https://vitela.javerianacali.edu.co/handle/11522/495Prion disease are entities of unknown genetic origin that cause in human beings a number of neurological manifestations that lead patients to states of immobility and severe deterioration, with a very poor prognosis and uncertain cure rates. It is difficult to find in the literature important findings to determine the clinical diagnosis and pharmacological methodology to counteract the deterioration of patients suffering from this condition. Therefore, a systematic search was carried out in the PubMed database. Research from 1990 to 2020 that addressed the diagnostic criteria of Creutzfeldt-Jackobs disease in adults, its clinical manifestations, diagnosis and management, recommendations and management guidelines were included to demonstrate the situation of patients who present this type of alterations and deterioration neurological diagnosis of difficult diagnosis, to determine clinical criteria that can give a clinical orientation for the diagnosis of these entities.La enfermedad por priones, son entidades de origen genético desconocido que ocasiona en los seres humano un sin número de manifestaciones neurológicas que llevan a los pacientes a estados de inmovilidad y deterioro severo, con muy mal pronóstico y con tasas curativas inciertas. Es difícil encontrar en la literatura hallazgos importantes para determinar el diagnóstico clínico y metodología farmacológica para contrarrestar el deterioro de los pacientes que sufren dicha afección. Por lo anterior Se realizó una búsqueda sistemática en la base de datos PubMed. Se incluyeron investigaciones desde 1990 hasta 2020 que abordaran los criterios diagnósticos de la enfermedad por Creutzfeldt-Jackobs en adultos, sus manifestaciones clínicas, diagnóstico y manejo, recomendaciones y guías de manejo para evidenciar la situación de los pacientes quienes presentan este tipo de alteraciones y deterioro neurológico de difícil diagnóstico, para determinar criterios clínicos que puedan dar una orientación clínica para el diagnóstico de estas entidades.application/pdfspaPontificia Universidad Javeriana Calihttps://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/695/591Derechos de autor 2023 Salutem Scientia Spiritushttps://creativecommons.org/licenses/by-nc-nd/4.0Salutem Scientia Spiritus; Vol. 8 No. 1 (2022): Revista Salutem Scientia Spiritus; 66-72Salutem Scientia Spiritus; Vol. 8 Núm. 1 (2022): Revista Salutem Scientia Spiritus; 66-722463-1426Deterioro neurológicoPrionesManifestaciones clínicasEncefalitisNeurological deteriorationPrionsClinical manifestationsEncephalitisPrion disease: Review of the literature.Enfermedad por priones: Revisión de la literatura.info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRevisión de la literatura11522/495oai:vitela.javerianacali.edu.co:11522/4952024-06-25 05:12:43.092metadata.onlyhttps://vitela.javerianacali.edu.coRepositorio Vitelavitela.mail@javerianacali.edu.co
dc.title.en-US.fl_str_mv	Prion disease: Review of the literature.
dc.title.es-ES.fl_str_mv	Enfermedad por priones: Revisión de la literatura.
title	Prion disease: Review of the literature.
spellingShingle	Prion disease: Review of the literature. Hernández, Jonattan Deterioro neurológico Priones Manifestaciones clínicas Encefalitis Neurological deterioration Prions Clinical manifestations Encephalitis
title_short	Prion disease: Review of the literature.
title_full	Prion disease: Review of the literature.
title_fullStr	Prion disease: Review of the literature.
title_full_unstemmed	Prion disease: Review of the literature.
title_sort	Prion disease: Review of the literature.
dc.creator.none.fl_str_mv	Hernández, Jonattan Zaninovich-Ruiz, Miliza Valencia, Henry
author	Hernández, Jonattan
author_facet	Hernández, Jonattan Zaninovich-Ruiz, Miliza Valencia, Henry
author_role	author
author2	Zaninovich-Ruiz, Miliza Valencia, Henry
author2_role	author author
dc.subject.es-ES.fl_str_mv	Deterioro neurológico Priones Manifestaciones clínicas Encefalitis
topic	Deterioro neurológico Priones Manifestaciones clínicas Encefalitis Neurological deterioration Prions Clinical manifestations Encephalitis
dc.subject.en-US.fl_str_mv	Neurological deterioration Prions Clinical manifestations Encephalitis
description	Prion disease are entities of unknown genetic origin that cause in human beings a number of neurological manifestations that lead patients to states of immobility and severe deterioration, with a very poor prognosis and uncertain cure rates. It is difficult to find in the literature important findings to determine the clinical diagnosis and pharmacological methodology to counteract the deterioration of patients suffering from this condition. Therefore, a systematic search was carried out in the PubMed database. Research from 1990 to 2020 that addressed the diagnostic criteria of Creutzfeldt-Jackobs disease in adults, its clinical manifestations, diagnosis and management, recommendations and management guidelines were included to demonstrate the situation of patients who present this type of alterations and deterioration neurological diagnosis of difficult diagnosis, to determine clinical criteria that can give a clinical orientation for the diagnosis of these entities.
publishDate	2022
dc.date.accessioned.none.fl_str_mv	2023-10-11T04:35:10Z
dc.date.available.none.fl_str_mv	2023-10-11T04:35:10Z
dc.date.none.fl_str_mv	2022-04-30
dc.type.none.fl_str_mv	info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion
dc.type.es-ES.fl_str_mv	Revisión de la literatura
status_str	publishedVersion
dc.identifier.none.fl_str_mv	https://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/695
dc.identifier.uri.none.fl_str_mv	https://vitela.javerianacali.edu.co/handle/11522/495
url	https://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/695 https://vitela.javerianacali.edu.co/handle/11522/495
dc.language.none.fl_str_mv	spa
language	spa
dc.relation.none.fl_str_mv	https://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/695/591
dc.rights.es-ES.fl_str_mv	Derechos de autor 2023 Salutem Scientia Spiritus https://creativecommons.org/licenses/by-nc-nd/4.0
rights_invalid_str_mv	Derechos de autor 2023 Salutem Scientia Spiritus https://creativecommons.org/licenses/by-nc-nd/4.0
dc.format.none.fl_str_mv	application/pdf
dc.publisher.es-ES.fl_str_mv	Pontificia Universidad Javeriana Cali
dc.source.en-US.fl_str_mv	Salutem Scientia Spiritus; Vol. 8 No. 1 (2022): Revista Salutem Scientia Spiritus; 66-72
dc.source.es-ES.fl_str_mv	Salutem Scientia Spiritus; Vol. 8 Núm. 1 (2022): Revista Salutem Scientia Spiritus; 66-72
dc.source.none.fl_str_mv	2463-1426
institution	Pontificia Universidad Javeriana Cali
repository.name.fl_str_mv	Repositorio Vitela
repository.mail.fl_str_mv	vitela.mail@javerianacali.edu.co
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Prion disease: Review of the literature.

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