Evidence map›Paper›PMID 37234314›Full record

ArticleJournal of oral and maxillofacial pathology : JOMFP

Consanguineous marriage as a key indicator of isolated congenital dental anomaly among South Indian population - A cross-sectional study.

M R C Rajeswari, Ananthalakshmi Ramamoorthy, A Rajakumar, V Keerthi Narayan

Open access · greenAbstract read
In one paragraph

Article in Journal of oral and maxillofacial pathology : JOMFP. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

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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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

M R C RajeswariDepartment of Oral Pathology and Microbiology, Priyadharshini Dental College and Hospital, Chennai, Tamil Nadu, India.
Ananthalakshmi RamamoorthyDepartment of Oral Pathology and Microbiology, Dr. MGR Educational and Research Institute, Thai Moogambigai Dental College and Hospital, Chennai, Tamil Nadu, India.
A RajakumarDepartment of Physical Medicine and Rehabilitation, Madras Medical College, Chennai, Tamil Nadu, India.
V Keerthi NarayanDepartment of Oral Pathology and Microbiology, Dr. MGR Educational and Research Institute, Thai Moogambigai Dental College and Hospital, Chennai, Tamil Nadu, India.
Dr. M.G.R. Educational and Research Institute · INMadras Medical College · INRagas Dental College & Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Orofacial anomalies occur due to incomplete fusion of developmental lines in the head and neck region. Dental anomalies regarded as the most common orofacial anomalies either in isolated or syndromic forms arise due to genetic and environmental factors. Among genetic influences, consanguineous marriages are considered as a significant predisposition factor in the transmission of congenital defects and several autosomal recessive diseases from one generation to other with an increased risk of detrimental effects on offspring. Aim: The present study was aimed to evaluate the prevalence and significant association between consanguinity and isolated dental anomalies with that of nonconsanguineous parents among south-Indian population. Methodology: A total of 116 participants with and without dental anomalies in isolated form pertaining to tooth size, shape, altered morphology, number and eruption were selected followed by brief case history. Participants with a positive history of consanguinity were categorized as Group A while others were categorized under Group B. Results: Sixty-four out of 116 participants (55.17%) showed positive consanguinity (Group A) among which 18 females (56%) and 14 males (44%) presented with isolated dental anomalies. 12 females (66.6%) and 9 males (64.2%) in Group A showed significance with first cousin ( Conclusion: A positive correlation between dental anomalies among offspring of consanguineous marriages revealed such prevalence may be attributed to increased risk of recessive deleterious gene expression or defective allele carried to offspring.

Indexed as

Consanguinitydefective alleledental anomaliesfirst cousingene transferrecessive disorders

Identifiers

PMID37234314
PMCPMC10207200
OpenAlexW4367154569

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.