Dentinogenesis Imperfecta

An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.

Also Known As:

Capdepont Teeth; Dentinogenesis Imperfecta 1; Dentinogenesis Imperfecta without Osteogenesis Imperfecta; Dentinogenesis Imperfecta, Shields Type 2; Dentinogenesis Imperfecta, Shields Type II; Opalescent Dentin; Opalescent Teeth without Osteogenesis Imperfecta; Dentin, Opalescent; Opalescent Dentin, Hereditary; Teeth, Capdepont; Hereditary Opalescent Dentin

Stomatognathic Diseases: 705
- Tooth Diseases: 33
  - Tooth Abnormalities: 33
    - Dentinogenesis Imperfecta: 134
- Stomatognathic System Abnormalities
  - Tooth Abnormalities: 33
    - Dentinogenesis Imperfecta: 134
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Stomatognathic System Abnormalities
    - Tooth Abnormalities: 33
      - Dentinogenesis Imperfecta: 134

C Russell Mack Selected Research

C Russell Mack Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure