Amelogenesis Imperfecta

A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.

Also Known As:

Congenital Enamel Hypoplasia

Stomatognathic Diseases: 705
- Tooth Diseases: 33
  - Tooth Abnormalities: 33
    - Developmental Defects of Enamel: 166
      - Amelogenesis Imperfecta: 276
- Stomatognathic System Abnormalities
  - Tooth Abnormalities: 33
    - Developmental Defects of Enamel: 166
      - Amelogenesis Imperfecta: 276
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Stomatognathic System Abnormalities
    - Tooth Abnormalities: 33
      - Developmental Defects of Enamel: 166
        Amelogenesis Imperfecta: 276

I Saroğlu Selected Research

I Saroğlu Research Topics

Disease

Drug/Important Bio-Agent (IBA)