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Creutzfeldt–Jakob disease: A case report and differential diagnoses
Although sporadic Creutzfeldt–Jakob disease is a rare neurodegenerative disease and often difficult to diagnose at the earliest onset, meticulous clinical examination, electroencephalography, and neuroimaging findings will help in diagnosis.
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364331/ https://www.ncbi.nlm.nih.gov/pubmed/35957791 http://dx.doi.org/10.1002/ccr3.6239 |
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author | Raut, Akash Thapa, Anjila Shrestha, Ashish Saud, Kamal Rajbhandari, Reema Katwal, Shailendra |
author_facet | Raut, Akash Thapa, Anjila Shrestha, Ashish Saud, Kamal Rajbhandari, Reema Katwal, Shailendra |
author_sort | Raut, Akash |
collection | PubMed |
description | Although sporadic Creutzfeldt–Jakob disease is a rare neurodegenerative disease and often difficult to diagnose at the earliest onset, meticulous clinical examination, electroencephalography, and neuroimaging findings will help in diagnosis. |
format | Online Article Text |
id | pubmed-9364331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93643312022-08-10 Creutzfeldt–Jakob disease: A case report and differential diagnoses Raut, Akash Thapa, Anjila Shrestha, Ashish Saud, Kamal Rajbhandari, Reema Katwal, Shailendra Clin Case Rep Case Report Although sporadic Creutzfeldt–Jakob disease is a rare neurodegenerative disease and often difficult to diagnose at the earliest onset, meticulous clinical examination, electroencephalography, and neuroimaging findings will help in diagnosis. John Wiley and Sons Inc. 2022-08-10 /pmc/articles/PMC9364331/ /pubmed/35957791 http://dx.doi.org/10.1002/ccr3.6239 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Raut, Akash Thapa, Anjila Shrestha, Ashish Saud, Kamal Rajbhandari, Reema Katwal, Shailendra Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title |
Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title_full |
Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title_fullStr |
Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title_full_unstemmed |
Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title_short |
Creutzfeldt–Jakob disease: A case report and differential diagnoses |
title_sort | creutzfeldt–jakob disease: a case report and differential diagnoses |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364331/ https://www.ncbi.nlm.nih.gov/pubmed/35957791 http://dx.doi.org/10.1002/ccr3.6239 |
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