Evidence map›Paper›PMID 42827664›Full record

ArticleClinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology2026

Syndromic diabetes and hypergonadotropic hypogonadism in a boy with a 12q24.31-32 chromosomal deletion involving

Tomohiro Nakagawa, Dai Saito, Hirohito Shima, Sayaka Kawashima, Dai Suzuki, Noriko Togashi, Atsuo Kikuchi, Junko Kanno

Abstract readCase Reports
In one paragraph

Article in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2026. 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
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.

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

8 authors.

Tomohiro NakagawaDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Dai Saito
Hirohito ShimaDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Sayaka KawashimaDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Dai SuzukiDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Noriko TogashiDepartment of Pediatric Neurology, Miyagi Children's Hospital, Sendai, Japan.
Atsuo KikuchiDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Junko KannoDepartment of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosomal deletions involving several disease-associated genes exhibit diverse phenotypes.

Indexed as

chromosomal deletionDHX37HNF1AMODYSETD1B

Identifiers

PMID42827664
PMCPMC13631439

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.