Evidence map›Paper›PMID 38807857›Full record

ArticlePathology oncology research : POR2024

Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis.

Gréta Antal, Anna Zsigmond, Ágnes Till, Eniko Orsi, Ildiko Szanto, Gergely Büki, László Kereskai, Zsuzsanna Herbert, Kinga Hadzsiev, Judit Bene

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

Article in Pathology oncology research : POR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Heterogeneity of Orodental Features in a Family with Noonan Syndrome.International journal of molecular sciences · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Review
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

10 authors.

Gréta AntalDepartment of Dentistry, Oral and Maxillofacial Surgery, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Anna ZsigmondDepartment of Medical Genetics, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Ágnes TillDepartment of Medical Genetics, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Eniko OrsiDepartment of Dentistry, Oral and Maxillofacial Surgery, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Ildiko SzantoDepartment of Dentistry, Oral and Maxillofacial Surgery, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Gergely BükiDepartment of Medical Genetics, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
László KereskaiDepartment of Pathology, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Zsuzsanna HerbertDepartment of Medical Imaging, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Kinga HadzsievDepartment of Medical Genetics, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.
Judit BeneDepartment of Medical Genetics, Clinical Center, Medical School, University of Pécs, Pécs, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Gardner SyndromeGenetic TestingAdolescentEarly DiagnosisFemaleHumansPedigreeTooth AbnormalitiesAPC genedental abnormalitiesGardner syndromeosteomaWES

Identifiers

PMID38807857
PMCPMC11130347

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.