Evidence map›Paper›PMID 41923794›Full record

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

Two siblings with Schaaf-Yang syndrome treated with growth hormone.

Yukiko Hashimoto, Kazutaka Nanba, Yosuke Konishi, Takashi Matsukura, Naoko Yano, Takeshi Yoshida

Abstract readCase Reports
PubMed Full text at PMC Publisher
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

6 authors.

Yukiko HashimotoDepartment of Pediatrics, NHO Kyoto Medical Center, Kyoto, Japan.
Kazutaka NanbaDivision of Clinical Genetics, NHO Kyoto Medical Center, Kyoto, Japan.
Yosuke KonishiDivision of Clinical Genetics, NHO Kyoto Medical Center, Kyoto, Japan.
Takashi MatsukuraDepartment of Pediatrics, NHO Kyoto Medical Center, Kyoto, Japan.
Naoko YanoDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takeshi YoshidaDepartment of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schaaf-Yang syndrome (SYS) is a rare neurodevelopmental disorder with overlapping features with Prader-Willi syndrome (PWS). We report two Japanese siblings with SYS harboring a rare

Indexed as

GH deficiencyhypothalamic dysfunctionMAGEL2neurodevelopmental disorderSchaaf-Yang syndrome

Identifiers

PMID41923794
PMCPMC13038379

What OpenQuestion holds

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Registered trials

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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.