Neuronal intranuclear inclusion disease with recurrent encephalitis
This report underscores the importance of recognizing NIID in patients with recurrent encephalitis-like presentations and highlights the diagnostic utility of genetic testing in distinguishing it from conditions like mitochondrial encephalopathies.
Authors
- Juncang Wu (ORCID: https://orcid.org/0000-0002-2632-5757)
- Chongbo Zhao (ORCID: https://orcid.org/0000-0001-9481-1418)
- Jingzi ZhangBao (ORCID: https://orcid.org/0000-0002-5308-6325)
- Chenchen Li (ORCID: https://orcid.org/0000-0002-8047-186X)
- Chi Zhang (ORCID: https://orcid.org/0000-0002-1827-8137)
- Yue Zhang (ORCID: https://orcid.org/0000-0002-5373-5567)
- Chao Quan (ORCID: https://orcid.org/0000-0003-1040-3930)
- Xiang Li (ORCID: https://orcid.org/0000-0001-7352-5535)
Institutions
- Anhui Medical University (CN)
- Fudan University (CN)
- Second Affiliated Hospital of Anhui Medical University (CN)
- Huashan Hospital (CN)
Publication Details
- Journal
- BMC Neurology
- Published
- 2025-10-27
- DOI
- https://doi.org/10.1186/s12883-025-04453-5
- Citations
- 1
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.91