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[Multidisciplinary focus on dentinogenesis imperfecta type II. Clinical analysis. Ultrastructural and genetic
H Rivera1, B Terán, J Pinto Cisternas
1Facultad de Odontología, Universidad Central de Venezuela.
Acta Odontologica Venezolana
|May 1, 1990
Summary
Dentinogenesis imperfecta (DI) is a genetic disorder affecting teeth. This review details DI type II, an autosomal dominant condition, and stresses the need for a multidisciplinary approach for diagnosis and treatment.
Area of Science:
- Dental genetics
- Oral pathology
- Clinical dentistry
Context:
- Dentinogenesis imperfecta (DI) is a rare inherited condition affecting dentin formation.
- Understanding its clinical, radiological, histopathological, and genetic features is crucial for diagnosis and management.
Purpose:
- To review the key aspects of Dentinogenesis imperfecta (DI).
- To describe a family exhibiting DI and classify the specific type and inheritance pattern.
- To highlight the importance of a collaborative, multidisciplinary approach in managing DI.
Summary:
- A comprehensive review of Dentinogenesis imperfecta (DI) covers clinical, radiological, histopathological, and genetic factors.
- Analysis of an affected family identified the condition as DI type II, an autosomal dominant disorder with complete penetrance and variable expressivity.
- A multidisciplinary team, including pedodontists, oral pathologists, and geneticists, is essential for accurate diagnosis and effective treatment.
Impact:
- Provides a detailed classification and understanding of Dentinogenesis imperfecta type II.
- Emphasizes the critical role of a multidisciplinary approach in managing patients with DI.
- Contributes to improved diagnostic accuracy and treatment strategies for inherited dental anomalies.