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Anti-recoverin antibody positive Heidenhain variant CJD: a case report

The Heidenhain variant Creutzfeldt-Jakob disease (CJD) is characterized by isolated visual symptoms at disease onset, which may mimic numerous ophthalmological disorders. Anti-recoverin autoantibody can be found in patients with autoimmune-related retinopathies. The presence of this antibody with vi...

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Autores principales: Chung, Chi-Ting, Jao, Tun, Su, Jen-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283419/
https://www.ncbi.nlm.nih.gov/pubmed/37337645
http://dx.doi.org/10.1080/19336896.2023.2223527
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author Chung, Chi-Ting
Jao, Tun
Su, Jen-Jen
author_facet Chung, Chi-Ting
Jao, Tun
Su, Jen-Jen
author_sort Chung, Chi-Ting
collection PubMed
description The Heidenhain variant Creutzfeldt-Jakob disease (CJD) is characterized by isolated visual symptoms at disease onset, which may mimic numerous ophthalmological disorders. Anti-recoverin autoantibody can be found in patients with autoimmune-related retinopathies. The presence of this antibody with visual symptoms might be confusing in the early stages of the Heidenhain variant CJD. We describe the first case of an anti-recoverin antibody found in the Heidenhain variant CJD who presented with progressive blurred vision then memory deterioration proceeded later. This presentation reinforces the concept that the presence of the anti-recoverin antibody could not exclude the possibility of the Heidenhain variant of CJD in highly suspicious patients with initial isolated visual disturbance.
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spelling pubmed-102834192023-06-22 Anti-recoverin antibody positive Heidenhain variant CJD: a case report Chung, Chi-Ting Jao, Tun Su, Jen-Jen Prion Reports The Heidenhain variant Creutzfeldt-Jakob disease (CJD) is characterized by isolated visual symptoms at disease onset, which may mimic numerous ophthalmological disorders. Anti-recoverin autoantibody can be found in patients with autoimmune-related retinopathies. The presence of this antibody with visual symptoms might be confusing in the early stages of the Heidenhain variant CJD. We describe the first case of an anti-recoverin antibody found in the Heidenhain variant CJD who presented with progressive blurred vision then memory deterioration proceeded later. This presentation reinforces the concept that the presence of the anti-recoverin antibody could not exclude the possibility of the Heidenhain variant of CJD in highly suspicious patients with initial isolated visual disturbance. Taylor & Francis 2023-06-19 /pmc/articles/PMC10283419/ /pubmed/37337645 http://dx.doi.org/10.1080/19336896.2023.2223527 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Reports
Chung, Chi-Ting
Jao, Tun
Su, Jen-Jen
Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title_full Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title_fullStr Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title_full_unstemmed Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title_short Anti-recoverin antibody positive Heidenhain variant CJD: a case report
title_sort anti-recoverin antibody positive heidenhain variant cjd: a case report
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283419/
https://www.ncbi.nlm.nih.gov/pubmed/37337645
http://dx.doi.org/10.1080/19336896.2023.2223527
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