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A Case of Rapidly Progressive Dementia
Creutzfeldt-Jakob disease (CJD) is a very rare neurodegenerative disorder that usually presents as rapidly progressive dementia with an extremely poor prognosis. The diagnosis of CJD can be extremely challenging due to its rarity, manifestation with non-specific neurological symptoms, associated bro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947950/ https://www.ncbi.nlm.nih.gov/pubmed/35371628 http://dx.doi.org/10.7759/cureus.22507 |
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author | Thekkekarott Kuruvila, Arun Ranawat, Nishant Hegde, Nikita Arora, Alok |
author_facet | Thekkekarott Kuruvila, Arun Ranawat, Nishant Hegde, Nikita Arora, Alok |
author_sort | Thekkekarott Kuruvila, Arun |
collection | PubMed |
description | Creutzfeldt-Jakob disease (CJD) is a very rare neurodegenerative disorder that usually presents as rapidly progressive dementia with an extremely poor prognosis. The diagnosis of CJD can be extremely challenging due to its rarity, manifestation with non-specific neurological symptoms, associated broad differentials, and a need for extensive workup. Awareness of disease-specific biomarkers, radiological signs, and diagnostic criteria are crucial for timely diagnosis. Here, we report a case of CJD, which presented as an atypical movement disorder that progressed to dementia and failure to thrive within a few weeks of presentation. |
format | Online Article Text |
id | pubmed-8947950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-89479502022-04-01 A Case of Rapidly Progressive Dementia Thekkekarott Kuruvila, Arun Ranawat, Nishant Hegde, Nikita Arora, Alok Cureus Internal Medicine Creutzfeldt-Jakob disease (CJD) is a very rare neurodegenerative disorder that usually presents as rapidly progressive dementia with an extremely poor prognosis. The diagnosis of CJD can be extremely challenging due to its rarity, manifestation with non-specific neurological symptoms, associated broad differentials, and a need for extensive workup. Awareness of disease-specific biomarkers, radiological signs, and diagnostic criteria are crucial for timely diagnosis. Here, we report a case of CJD, which presented as an atypical movement disorder that progressed to dementia and failure to thrive within a few weeks of presentation. Cureus 2022-02-22 /pmc/articles/PMC8947950/ /pubmed/35371628 http://dx.doi.org/10.7759/cureus.22507 Text en Copyright © 2022, Thekkekarott Kuruvila et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Thekkekarott Kuruvila, Arun Ranawat, Nishant Hegde, Nikita Arora, Alok A Case of Rapidly Progressive Dementia |
title | A Case of Rapidly Progressive Dementia |
title_full | A Case of Rapidly Progressive Dementia |
title_fullStr | A Case of Rapidly Progressive Dementia |
title_full_unstemmed | A Case of Rapidly Progressive Dementia |
title_short | A Case of Rapidly Progressive Dementia |
title_sort | case of rapidly progressive dementia |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947950/ https://www.ncbi.nlm.nih.gov/pubmed/35371628 http://dx.doi.org/10.7759/cureus.22507 |
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