Heterogeneity of Orodental Features in a Family with Noonan Syndrome
Gréta Antal, Laura Csabai, Anna Zsigmond, Ildiko Szanto, Kinga Hadzsiev, Judit Bene · 2025
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Description
A peer-reviewed research article from Europe PMC (2025). Noonan syndrome is a relatively common genetic syndrome with clinical and genetic heterogeneity. Besides the characteristic features such as short stature, typical facial features, congenital heart defects, skeletal and ocular anomalies, various orodental manifestations occur with variable frequency. High-arched palate, malocclusions, micrognathism, giant cell lesions, and anomalous lateral incisors are frequently observed features, whereas supernumerary teeth, hypodontia, macrodontia, enamel hypoplasia, severe dental caries, impacted teeth, delayed eruption, taurodontism and odontoma have occasionally been reported.
Catalog record
| CREATOR | Gréta Antal, Laura Csabai, Anna Zsigmond, Ildiko Szanto, Kinga Hadzsiev, Judit Bene |
|---|---|
| YEAR | 2025 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 18 KB |
| VERSION | 1.0 |
| LICENSE | CC BY 4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |