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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...

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Detalles Bibliográficos
Autores principales: Thekkekarott Kuruvila, Arun, Ranawat, Nishant, Hegde, Nikita, Arora, Alok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
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.
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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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