Evidence map›Paper›PMID 39452687›Full record

ArticleNeurology international2024

Adult Case of Pontocerebellar Hypoplasia without the Claustrum.

Koji Hayashi, Shiho Mitsuhashi, Ei Kawahara, Asuka Suzuki, Yuka Nakaya, Mamiko Sato, Yasutaka Kobayashi

Abstract readCase Reports
In one paragraph

Article in Neurology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Multiscale characterization of the human claustrum from histology to MRI.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Koji HayashiDepartment of Rehabilitation Medicine, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.ORCID 0000-0003-3446-0913
Shiho MitsuhashiDepartment of Rehabilitation Medicine, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.
Ei KawaharaDepartment of Pathology, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.
Asuka SuzukiDepartment of Rehabilitation Medicine, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.
Yuka NakayaDepartment of Rehabilitation Medicine, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.
Mamiko SatoDepartment of Rehabilitation Medicine, Fukui General Hospital, 55-16-1 Egami, Fukui 910-8561, Japan.ORCID 0000-0002-2947-9743
Yasutaka KobayashiGraduate School of Health Science, Fukui Health Science University, 55-13-1 Egami, Fukui 910-3190, Japan.ORCID 0000-0002-6305-2444

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe the case of a 63-year-old man with pontocerebellar hypoplasia without the claustrum (CL). The patient had a history of cerebral palsy, intelligent disability, cerebellar atrophy, and seizures since birth. At age 61, brain computed tomography (CT) revealed significant cerebellar and brainstem atrophy. At age 63, he was admitted to our hospital for aspiration pneumonia. Although he was treated with medications, including antibiotics, he died one month after admission. The autopsy revealed a total brain weight of 815 g, with the small-sized frontal lobe, cerebellum, and pons. The cross-section of the fourth ventricle had a slit-like appearance, rather than the typical diamond shape. In addition, bilateral CLs were not observed. Apart from CL, no other missing brain tissue or cells could be identified. Microscopic examinations disclosed neurofibrillary tangles in the hippocampus but not in the cortex; however, neither senile plaques nor Lewy bodies were detected. No acquired lesions, including cerebral infarction, hemorrhage, or necrosis, were noted. We pathologically diagnosed the patient with pontocerebellar hypoplasia without CL. As there have been no prior reports of pontocerebellar hypoplasia lacking CL in adults, this case may represent a new subtype. Congenital CL deficiency is likely associated with abnormalities in brain development. CL may play a role in seizure activity, and the loss of bilateral CLs does not necessarily result in immediate death. Further studies are needed to clarify the functions of CL.

Indexed as

adultclaustrumpontocerebellar hypoplasia

Identifiers

PMID39452687
PMCPMC11510225

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.