Evidence map›Paper›PMID 40895890›Full record

ArticleCureus2025

Cleidocranial Dysplasia With Multiple Impacted Teeth and Dentigerous Cysts: A Case Report of a Rare Entity.

Manhar Shinh

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

1 author.

Manhar ShinhDepartment of Dentistry, Adesh Institute of Dental Sciences and Research, Bathinda, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This report describes an unusual case of a 27-year-old male presenting with cleidocranial dysplasia (CCD), a rare genetic disorder affecting bone and dental development. The patient exhibited classic features, including short stature, drooping shoulders with hypermobility, broad forehead, maxillary deficiency, and mandibular prognathism. Intraoral examination revealed multiple missing teeth, retained deciduous teeth, and gingival swelling in the maxillary anterior region. Radiographic evaluation, including orthopantomogram and cone beam CT (CBCT), revealed 45 impacted permanent and supernumerary teeth, a rare finding, along with multiple dentigerous cysts, notably a large cyst in the right maxilla causing cortical plate breaches and nasal cavity displacement. Additional skeletal abnormalities included hypoplastic clavicles, open cranial sutures, and underdeveloped sinuses. Genetic testing confirmed a Runt-related transcription factor 2 (

Indexed as

cleidocranial dysplasiadentigerous cystmutationrunx2supernumerary teeth

Identifiers

PMID40895890
PMCPMC12397749

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.