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Dentinogenesis imperfecta type II: case report

A Modesto1, A C Alves, A R Vieira

  • 1Faculdade de Odontologia, Universidade Federal do Rio de Janeiro, Brasil.

Brazilian Dental Journal
|January 1, 1996
PubMed
Summary
This summary is machine-generated.

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Dentinogenesis imperfecta type II is a rare genetic disorder affecting teeth. This case study highlights the challenges in managing this condition.

Area of Science:

  • Dentistry
  • Genetics
  • Oral Pathology

Background:

  • Dentinogenesis imperfecta (DI) encompasses inherited disorders of dentin formation.
  • DI type II, also known as hereditary opalescent dentin, is characterized by abnormal dentin development.

Observation:

  • This report details a specific case of dentinogenesis imperfecta type II.
  • The case presentation includes clinical and radiographic findings.

Findings:

  • The study emphasizes the significant difficulties encountered in the clinical management and treatment of DI type II.
  • Treatment strategies for dentinogenesis imperfecta type II present unique challenges due to the compromised tooth structure.

Implications:

  • Understanding the complexities of DI type II is crucial for effective patient care.

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  • Further research into improved treatment modalities for dentinogenesis imperfecta is warranted.