Evidence map›Paper›PMID 36388612›Full record

ArticleRadiology case reports2023

Cleidocranial dysplasia with hypermobile Ehlers-Danlos syndrome: A case report.

Rengin Ibrahim, Omar Hamadah, Mahmoud Abdul-Hak, Aladdin Alshawa, Mohamad Alhasan Alouda

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Radiology case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 31% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Rengin IbrahimDepartment of Oral Medicine, Faculty of Dental Medicine, Damascus University, Meza Highway, Damascus, Syria.
Omar HamadahDepartment of Oral Medicine, Faculty of Dental Medicine, Damascus University, Meza Highway, Damascus, Syria.
Mahmoud Abdul-HakDepartment of Oral Medicine, Faculty of Dental Medicine, Damascus University, Meza Highway, Damascus, Syria.
Aladdin AlshawaDepartment of Oral Medicine, Faculty of Dental Medicine, Damascus University, Meza Highway, Damascus, Syria.
Mohamad Alhasan AloudaDepartment of Endodontics, Faculty of Dental Medicine, Damascus University, Damascus, Syria.
Damascus University · SY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cleidocranial dysplasia (CCD) is a rare genetic skeletal syndrome. The most common features are open fontanelles, hypertelorism, mid-face retrusion, hypoplasia, or aplasia of the clavicles leading to excessive shoulder mobility, dental abnormalities such as supernumerary, and impacted teeth. This case report describes a 31-year-old male with CCD with several unusual symptoms like generalized joint hypermobility, skin laxity, and smooth skin, which leads to set a diagnosis of hypermobile Ehlers-Danlos syndrome (hEDS). To our knowledge, this is the first case report in the literature that describes a patient with these 2 distinct syndromes CCD and hEDS.

Indexed as

Computed tomographyJoint hypermobilityOpen fontanellesSkin laxitySupernumerary teeth

Identifiers

PMID36388612
PMCPMC9649364
OpenAlexW4308428485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.