Evidence map›Paper›PMID 40105472›Full record

ReviewJournal of clinical research in pediatric endocrinology2026

Clinical and Molecular Landscape of Weiss-Kruszka Syndrome: A Case Report and Literature Review

Lele Li, Chunxiu Gong

Abstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Journal of clinical research in 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

2 authors.

Lele LiBeijing Children’s Hospital, the Capital Medical University, National Center for Children’s Health, Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing, ChinaORCID 0000-0001-8291-6810
Chunxiu GongBeijing Children’s Hospital, the Capital Medical University, National Center for Children’s Health, Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing, ChinaORCID 0000-0002-1262-7383

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Weiss-Kruszka syndrome (WSKA; OMIM#618619) is a rare condition with multiple congenital anomalies. This study describes a patient with WSKA from Northern China. The patient was a 9.75-year-old boy who presented with growth retardation (growth velocity: 3-4 cm/year at school age), delayed motor and speech development, and eating difficulty. The patient’s weight was 22 kg (<3

Indexed as

Abnormalities, MultipleGrowth DisordersChildHumansMalePhenotypegenotypicphenotypicWeiss-Kruszka syndromeZNF462 gene

Identifiers

PMID40105472
PMCPMC13197104

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.