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Dentinogenesis Imperfecta Summary

Description: 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: Dentin, Hereditary Opalescent; Dentinogenesis Imperfectas; Dentins, Hereditary Opalescent; Hereditary Opalescent Dentins; Imperfecta, Dentinogenesis Show All >>

Networked: 85 relevant articles (0 outcomes, 13 trials/studies) for this Disease

Key Drugs and Agents for Dentinogenesis Imperfecta

Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
  1. Collagen : 3 studies in 9 results : IBA
  2. dentin sialophosphoprotein : 2 studies in 22 results : IBA
  3. Amino Acids : 1 study in 3 results : FDA 53
  4. Opalescent dentin : 1 study in 3 results : IBA
  5. Nonsense Codon (Nonsense Mutation) : 1 study in 2 results : IBA
  6. Protein Sorting Signals (Signal Peptide) : 1 study in 1 result : IBA
  7. Calcitriol Receptors (Calcitriol Receptor) : 1 study in 1 result : IBA
  8. Diamond : 1 study in 1 result : IBA
  9. Complementary DNA (cDNA) : 1 study in 1 result : IBA
  10. Tyrosine (L-Tyrosine) : 1 study in 1 result : FDA 12
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Diseases Related to Dentinogenesis Imperfecta

  1. Osteogenesis Imperfecta (Lobstein Disease)
  2. Anodontia
  3. Metabolic Bone Diseases (Osteopenia)
  4. Dentin Dysplasia
  5. Amelogenesis Imperfecta
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Key Therapies for Dentinogenesis Imperfecta

Efficacy Chart >>
  1. Prosthodontics : 1 study in 2 results
  2. Overlay Denture : 6 results
  3. Mouth Rehabilitation : 4 results
  4. Transplants (Transplant) : 1 result
  5. Synchrotrons : 1 result
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