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Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review

Neuronal nuclear inclusion disease (NIID) is a rare and chronic progressive neurological degenerative disease. We presented a 68‐year‐old man with paroxysmal orientation disorder 1 year prior, mental and behavioral disorders for 2 days, and confirmed the diagnosis of NIID with skin biopsy. We sugges...

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Autores principales: Lou, Yue, Yu, Jing‐Ying, Shuai, Zhi‐Feng, Zhao, Ting, Wang, Yan‐Wen, Liu, Xiao‐Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805289/
https://www.ncbi.nlm.nih.gov/pubmed/36606264
http://dx.doi.org/10.1002/agm2.12237
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author Lou, Yue
Yu, Jing‐Ying
Shuai, Zhi‐Feng
Zhao, Ting
Wang, Yan‐Wen
Liu, Xiao‐Li
author_facet Lou, Yue
Yu, Jing‐Ying
Shuai, Zhi‐Feng
Zhao, Ting
Wang, Yan‐Wen
Liu, Xiao‐Li
author_sort Lou, Yue
collection PubMed
description Neuronal nuclear inclusion disease (NIID) is a rare and chronic progressive neurological degenerative disease. We presented a 68‐year‐old man with paroxysmal orientation disorder 1 year prior, mental and behavioral disorders for 2 days, and confirmed the diagnosis of NIID with skin biopsy. We suggest that patients with atypical clinical symptoms showed characteristic high signal in the dermatomedullary junction on DWI; NIID should be considered.[Image: see text]
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spelling pubmed-98052892023-01-04 Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review Lou, Yue Yu, Jing‐Ying Shuai, Zhi‐Feng Zhao, Ting Wang, Yan‐Wen Liu, Xiao‐Li Aging Med (Milton) Case Report Neuronal nuclear inclusion disease (NIID) is a rare and chronic progressive neurological degenerative disease. We presented a 68‐year‐old man with paroxysmal orientation disorder 1 year prior, mental and behavioral disorders for 2 days, and confirmed the diagnosis of NIID with skin biopsy. We suggest that patients with atypical clinical symptoms showed characteristic high signal in the dermatomedullary junction on DWI; NIID should be considered.[Image: see text] John Wiley and Sons Inc. 2022-12-20 /pmc/articles/PMC9805289/ /pubmed/36606264 http://dx.doi.org/10.1002/agm2.12237 Text en © 2022 The Authors. Aging Medicine published by Beijing Hospital and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Report
Lou, Yue
Yu, Jing‐Ying
Shuai, Zhi‐Feng
Zhao, Ting
Wang, Yan‐Wen
Liu, Xiao‐Li
Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title_full Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title_fullStr Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title_full_unstemmed Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title_short Adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: A case report and literature review
title_sort adult‐onset neuronal nuclear inclusion disease presenting with mental and behavioral disorders: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805289/
https://www.ncbi.nlm.nih.gov/pubmed/36606264
http://dx.doi.org/10.1002/agm2.12237
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