# Oral Manifestations in Adolescents with Genetic Syndromes: A Retrospective Cross-Sectional Study

**Authors:** Adriana Țenț, Raluca Iurcov, Abel Emanuel Moca, Rahela Tabita Moca, Ioan Andrei Țig, Ruxandra Ilinca Matei

PMC · DOI: 10.3390/jcm14207217 · Journal of Clinical Medicine · 2025-10-13

## TL;DR

This study found that most adolescents with genetic syndromes have dental issues like missing teeth and abnormal tooth shapes, which could help in diagnosing these conditions.

## Contribution

The study identifies specific dental anomaly patterns in genetic syndromes and their potential as diagnostic markers.

## Key findings

- Dental anomalies were present in 68% of adolescents with genetic syndromes.
- Hypodontia, taurodontism, and enamel hypoplasia were the most common dental anomalies observed.

## Abstract

Background/Objectives: Few studies have comprehensively examined dental anomalies in adolescents with genetic syndromes. This study aimed to assess their prevalence, types, and clinical patterns in a diverse sample of genetically confirmed cases. Methods: We conducted a retrospective cross-sectional study of 213 patients aged 12 to 18 years with various genetic syndromes, using clinical data originally collected between 2011 and 2014 at a tertiary center. Clinical examinations were complemented by radiographs when available. Anomalies were categorized by type, and a disproportionality analysis (Rate of Occurrence Ratio, ROR) quantified risk relative to syndrome representation. Results: Dental anomalies were present in 68% of adolescents. The most common findings were hypodontia, taurodontism (9%), and enamel hypoplasia (8%). Nearly half of the patients exhibited combined patterns, with hypodontia–taurodontism as the most characteristic combination (14%). Prevalence was particularly high in trisomy-based (80%) and osteogenesis-related (100%) syndromes. Down syndrome showed the strongest association (ROR 3.95; 95% CI: 2.15–7.25), while some conditions such as Turner, Ehlers-Danlos, and Tuberous sclerosis displayed significantly lower rates. Conclusions: Dental anomalies are both highly prevalent and patterned in adolescents with genetic syndromes. Their co-occurrence and specificity suggest that they may serve as useful diagnostic markers in syndromic evaluation.

## Linked entities

- **Diseases:** Down syndrome (MONDO:0008608), Tuberous sclerosis (MONDO:0001734)

## Full-text entities

- **Diseases:** osteogenesis-related (MESH:D010013), taurodontism (MESH:C536946), Ehlers-Danlos (MESH:D004535), syndromes (MESH:D013577), Turner (MESH:D014424), enamel hypoplasia (MESH:D003744), Down syndrome (MESH:D004314), Dental anomalies (OMIM:614188), Tuberous sclerosis (MESH:D014402), hypodontia (MESH:D000848), Genetic Syndromes (MESH:D030342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12565033/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12565033/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12565033/full.md

---
Source: https://tomesphere.com/paper/PMC12565033