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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...
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/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] |
format | Online Article Text |
id | pubmed-9805289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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