Evidence map›Paper›PMID 35428363›Full record

ReviewJournal of medical case reports2022

Wisconsin syndrome with brain volume laterality: a case report and review of the literature.

Satomi Okano, Yoshio Makita, Kayano Kimura, Ikue Fukuda, Akie Miyamoto, Hajime Tanaka

Open access · goldAbstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Journal of medical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 96% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Satomi OkanoDepartment of Pediatrics, Hokkaido Asahikawa Habilitation Center for Children, 2-1-1-43 Shunkodai Asahikawa, Hokkaido, 071-8142, Japan. s-okano@ceres.dti.ne.jp.ORCID http://orcid.org/0000-0002-2756-6114
Yoshio MakitaDepartment of Genetic Counseling, Asahikawa Medical University Hospital, Hokkaido, Japan.
Kayano KimuraDepartment of Pediatrics, Hokkaido Asahikawa Habilitation Center for Children, 2-1-1-43 Shunkodai Asahikawa, Hokkaido, 071-8142, Japan.
Ikue FukudaDepartment of Pediatrics, Hokkaido Asahikawa Habilitation Center for Children, 2-1-1-43 Shunkodai Asahikawa, Hokkaido, 071-8142, Japan.
Akie MiyamotoDepartment of Pediatrics, Hokkaido Asahikawa Habilitation Center for Children, 2-1-1-43 Shunkodai Asahikawa, Hokkaido, 071-8142, Japan.
Hajime TanakaDepartment of Pediatrics, Hokkaido Asahikawa Habilitation Center for Children, 2-1-1-43 Shunkodai Asahikawa, Hokkaido, 071-8142, Japan.
Asahikawa University · JPAsahikawa Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWisconsin syndrome is a congenital anomaly caused by a 3q interstitial deletion. It is associated with characteristic facies and developmental delays. Only 33 cases with a deletion estimated to be in the associated region 3q25 have been reported. CASE REPORT: We present the case of a 5-year-old Japanese girl with a 3q24q25.2 deletion. Her facial features corresponded to the Wisconsin syndrome phenotype, and she exhibited brain volume laterality, which has not been reported previously.

conclusionThe clinical features of our case may contribute to narrowing down the list of candidate genes of Wisconsin syndrome.

Indexed as

Chromosome AberrationsChromosome DeletionBrainFaciesFemaleHumansPhenotypeSyndromeWisconsin3q interstitial deletionBrain volume lateralityWisconsin syndromeWWTR1

Identifiers

PMID35428363
PMCPMC9013138
OpenAlexW4223990071

What OpenQuestion holds

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Registered trials

None linked

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.