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Dental agenesis in hemifacial microsomia
A Silvestri1, G Natali, M T Fadda
1Maxillo-Facial Surgery, Rome University La Sapienza, Italy.
Pediatric Dentistry
|January 1, 1996
Summary
Hemifacial microsomia (HM) is a congenital facial deformity. This study found that more severe HM cases correlate with a higher incidence of tooth agenesis, particularly in third molars.
Area of Science:
- Craniofacial anomalies
- Developmental biology
- Dental genetics
Background:
- Hemifacial microsomia (HM) is a congenital condition affecting facial asymmetry.
- It originates from abnormal development of the first and second branchial arches.
- Understanding dental anomalies in HM is crucial for treatment planning.
Purpose of the Study:
- To determine the incidence of tooth agenesis and dental inclusions in patients with Hemifacial microsomia.
- To explore potential correlations between HM severity and these dental anomalies.
Main Methods:
- Clinical examination of 63 HM patients (27 male, 36 female; ages 7-43).
- Analysis of photographs and radiographic data.
- Documentation of monolateral and bilateral HM presentations.
Main Results:
- Tooth agenesis was observed in 11 patients (at least one missing tooth on the affected side).
- Dental inclusions were noted in 5 patients.
- A positive correlation was found between HM severity and the likelihood of tooth agenesis.
- Third molars were the most frequently missing teeth.
- No significant relationship was found between HM severity and dental inclusions.
Conclusions:
- Tooth agenesis is a notable dental anomaly in Hemifacial microsomia patients.
- The severity of HM appears to influence the occurrence of tooth agenesis.
- Further research may elucidate the specific mechanisms linking HM severity to dental development.