Evidence map›Paper›PMID 41063794›Full record

ArticleCase reports in dentistry2025

Cherubism in a 4-Year-Old Boy: A Clinical, Radiological, and Genetic Report.

Menzile Seda Cosar, Kardelen Demirel, Ugur Baran Goz, Merih Seval Olmez

Abstract readCase Reports
In one paragraph

Article in Case reports in dentistry, 2025. 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

4 authors.

Menzile Seda CosarDepartment of Pediatric Dentistry, Hacettepe University Faculty of Dentistry, Ankara, Turkey.ORCID https://orcid.org/0000-0002-5400-1290
Kardelen DemirelDepartment of Pediatric Dentistry, Hacettepe University Faculty of Dentistry, Ankara, Turkey.ORCID https://orcid.org/0009-0009-6157-7528
Ugur Baran GozDepartment of Oral and Maxillofacial Surgery, Hacettepe University Faculty of Dentistry, Ankara, Turkey.ORCID https://orcid.org/0009-0000-6119-5938
Merih Seval OlmezDepartment of Pediatric Dentistry, Hacettepe University Faculty of Dentistry, Ankara, Turkey.ORCID https://orcid.org/0000-0002-9407-9447

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cherubism is a rare hereditary disorder, often referred to as familial fibrous dysplasia of the jaws, and is characterized by painless, bilaterally symmetrical enlargement of the facial structures. There are various clinical manifestations, ranging from the asymptomatic to the aggressive form. Since cherubism tends to regress spontaneously over time, therapeutic decisions are primarily guided by the severity of clinical presentation and individual patient needs. This case report highlights the clinical, radiological, and genetic findings of cherubism in a 4-year-old male patient.

Indexed as

cherubismcomputed tomographyfamilial fibrous dysplasiagiant cell granulomajaw expansion

Identifiers

PMID41063794
PMCPMC12503967

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.