Evidence map›Paper›PMID 22629068›Full record

ArticleContemporary clinical dentistry2012

Oral manifestations of Ellis-van Creveld syndrome.

Ritesh Kalaskar, Ashita R Kalaskar

Open access · goldAbstract readCase Reports
In one paragraph

Article in Contemporary clinical dentistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Navigating complexities: A pediatric case of Ellis-van Creveld syndrome.Journal of family medicine and primary care · 2025
    Article
  3. Article
  4. Dental Anomalies in Rare, Genetic Ciliopathic Disorder-A Case Report and Review of Literature.International journal of environmental research and public health · 2020
    Review
  5. Risk Factors for Obstructive Sleep Apnea Syndrome in Children: State of the Art.International journal of environmental research and public health · 2019
    Review
  6. Oral manifestations of ellis-van creveld syndrome. A rare case report.Journal of clinical and experimental dentistry · 2019
    Article
  7. Review
  8. Sleep-Disordered Breathing in Children with Rare Skeletal Disorders: A Survey of Clinical Records.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Chondroectodermal dysplasia: a rare syndrome.Journal of dentistry (Tehran, Iran) · 2014
    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

2 authors at 2 institutions in 1 country.

Ritesh KalaskarDepartment of Pedodontics, Government Dental College and Hospital, VSPM Dental College and Research Center, Nagpur, Maharashtra, India.
Ashita R Kalaskar
ACPM Dental College and Hospital · INGovernment Dental College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ellis-van Creveld syndrome is a rare autosomal-recessive disorder characterized by short limbs, post-axial polydactyly, ectodermal dysplasia, edentulous mandibular incisor region, absence of mucobuccal fold, congenitally missing teeth, slight serrations of the alveolar ridge and multiple small alveolar notches. The clinical report not only describes the classical oral and dental manifestations of Ellis-van Creveld syndrome but also presents unusual findings such as single-rooted and funnel-shaped primary first molars, single conical roots of primary second molars and taurodontisum, which must be considered in the differential diagnostic criteria to avoid misdiagnosis of syndromes. The article also discusses the differential diagnosis and preventive and therapeutic oral health care for these patients. The management of Ellis-van Creveld syndrome is multidisciplinary and, therefore, the oral health care provider should get updated with latest knowledge for timely referral to prevent the patient from further complications of heart defect and bony deformity.

Indexed as

Absence of mucobuccal foldalveolar notchesautosomal recessivegenu valgumpartial harelip

Identifiers

PMID22629068
PMCPMC3354796
OpenAlexW1973089312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.