Evidence map›Paper›PMID 41716662›Full record

ArticleFrontiers in neuroscience2026

Case Report: Distinctive features of cognitive dysfunction and amelioration by antiseizure medication in neuronal intranuclear inclusion disease.

Hiroya Ohara, Masami Yamanaka, Fumi Okada, Aiko Okazaki, Marisse Dy Dizon, Ajay Elangovan, Harysh Winster Suresh Babu, Mahalaxmi Iyer, Balachandar Vellingiri, Masako Kinoshita

Abstract readCase Reports
In one paragraph

Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Hiroya OharaDepartment of Neurology, Minaminara General Medical Center, Yoshino, Nara, Japan.
Masami YamanakaDepartment of Clinical Laboratory, Minaminara General Medical Center, Yoshino, Nara, Japan.
Fumi OkadaDepartment of Pathology and Diagnostics, Nara Medical University School of Medicine, Kashihara, Nara, Japan.
Aiko OkazakiDepartment of Dermatology, Minaminara General Medical Center, Yoshino, Nara, Japan.
Marisse Dy DizonDepartment of Neuroscience and Behavioral Medicine, University of Santo Tomas Hospital, Manila, Philippines.
Ajay ElangovanHuman Cytogenetics and Stem Cell Laboratory, Department of Zoology, Central University of Punjab, Bathinda, Punjab, India.
Harysh Winster Suresh BabuHuman Cytogenetics and Stem Cell Laboratory, Department of Zoology, Central University of Punjab, Bathinda, Punjab, India.
Mahalaxmi IyerDepartment of Microbiology, Central University of Punjab, Bathinda, Punjab, India.
Balachandar VellingiriHuman Cytogenetics and Stem Cell Laboratory, Department of Zoology, Central University of Punjab, Bathinda, Punjab, India.
Masako KinoshitaDepartment of Neurology, National Hospital Organization Utano National Hospital, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative disease. We investigated a role of nonconvulsive status epilepticus (NCSE) in cognitive dysfunction in pathologically confirmed NIID. We also analyzed distinctive factors to differentiate NIID from Alzheimer's disease (AD). Methods: A 63-year-old man presented with transient consciousness disturbance (Day 1). For previous 6 years he had been suffering from similar episodes and gradually progressive cognitive decline. Clinical characteristics and response to antiseizure medications (ASM) were analyzed with a narrative literature review. Results: Neurological examination showed disorientation, memory disturbance, aphasia, agraphia, and impaired visuospatial ability. On Day 27, his MMSE scored 10. Diffusion-weighted MRI showed high intensity signal in the corticomedullary junction of the frontal lobe, which could not explain his neurological manifestations. EEG showed seizure patterns arising from the bilateral occipital areas. ASM improved MMSE score to 23. Skin biopsy confirmed his diagnosis as dementia-dominant sporadic NIID. He died on Day 77. Cognitive dysfunction in visuospatial execution, manifested by impaired pentagon drawing and agraphia of both kanji (Japanese morphograms) and kana (Japanese syllabograms), its fluctuating course, and reactivity to ASM were clear distinction from AD. Conclusion: NCSE can accelerate cognitive decline and ASM can improve cognitive function in NIID. Cognitive evaluation using pentagon drawing and handwriting of both morphograms and syllabograms can be useful to differentiate NIID from AD.

Indexed as

agraphiaantiseizure medicationscognitive dysfunctiondementianeuronal intranuclear inclusion diseasenonconvulsive status epilepticusskin biopsyvisuospatial execution

Identifiers

PMID41716662
PMCPMC12913443

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