Evidence map›Paper›PMID 42163284›Full record

ArticleBMC oral health2026

Dental anomalies and dental age in children with down syndrome: a comparative retrospective study with healthy controls.

İsmail Cihangir, Esra Kizilci

Abstract readComparative Study
In one paragraph

Article in BMC oral health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

İsmail CihangirDepartment of Pediatric Dentistry, Faculty of Dentistry, Yozgat Bozok University, Yozgat, Turkey. ismail.cihangir@bozok.edu.tr.ORCID 0000-0002-7919-085X
Esra KizilciDepartment of Pediatric Dentistry, Faculty of Dentistry, Erciyes University, Kayseri, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with Down syndrome (DS) are known to present various dental anomalies; however, evaluating anomaly types together with dental age remains limited, in Turkish pediatric populations. The aim of this study was to investigate differences in dental anomaly prevalence and dental age between children with DS and healthy controls.

methodsThis retrospective study was conducted at a university dental clinic using panoramic radiographs obtained between 2009 and 2024. A total of 61 children with DS and 61 age and sex-matched healthy controls (5-14 years) were included. Dental anomalies were categorized as size, shape, number and structure on radiographic evaluation. Dental age was estimated using the Nolla method by assessing six mandibular teeth. Statistical analyses were performed using chi-square, Fisher's exact, Mann-Whitney U tests and p-value < 0.05 was considered statistically significant.

resultsDental anomalies were more prevalent in the DS group. Taurodontism was significantly more common in children with DS (36.1%, 95% CI: 24.2-48.0) compared to controls (19.7%, 95% CI: 9.7-29.7; p = 0.043). Hyperdontia (14.8% vs. 1.6%, p = 0.008), hypodontia (42.6% vs. 4.9%, p < 0.001), and combined hyperdontia and hypodontia (p < 0.001) were also significantly higher in the DS group. Structural anomalies (8.2% vs. 0%, p = 0.022), microdontia (59.0% vs. 11.5%, p < 0.001), and macrodontia (54.1% vs. 6.6%, p < 0.001) were observed more frequently in children with DS. Mean dental age was lower in the DS group (8.3±1.4 vs. 8.5±1.2; 95% CI: 7.95-8.65 vs. 8.20-8.80), although the difference was not statistically significant (p=0.605). Age-group analysis showed a significant difference only at 8 years of age (p=0.019).

conclusionsChildren with DS demonstrated a higher occurrence of dental anomalies than healthy peers. Although dental maturation appeared to be delayed in the DS group, the difference was not significant. These findings highlight the importance of individualized radiographic assessment in children with DS and may support more precise timing of preventive and interceptive dental interventions.

Indexed as

Age Determination by TeethDown SyndromeTooth AbnormalitiesAdolescentAnodontiaCase-Control StudiesChildChild, PreschoolDental Pulp CavityFemaleHumansMalePrevalenceRadiography, PanoramicRetrospective StudiesTooth, SupernumeraryDental ageDental anomaliesDown SyndromeSustainable Development Goal 3 (Good Health and Well-Being)

Identifiers

PMID42163284
PMCPMC13356790

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LicenceCC BY-NC-ND
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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.