Single upper central incisor

A hereditary autosomal dominant condition characterized primarily by single (unpaired) deciduous and permanent maxillary central incisors and short stature. Growth hormone deficiencies may also be present. Mutations in the SHH gene have been identified. OMIM: 147250

Also Known As:

Fused incisors; Incisors, Fused; SMMCI Solitary median maxillary central incisor; SMMCI Syndrome; Single central maxillary incisor; Solitary median maxillary central incisor; Solitary median maxillary central incisor syndrome

Stomatognathic Diseases: 705
- Tooth Diseases: 33
  - Tooth Abnormalities: 33
    - Anodontia: 374
      - Single upper central incisor: 11
- Stomatognathic System Abnormalities
  - Tooth Abnormalities: 33
    - Anodontia: 374
      - Single upper central incisor: 11
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Stomatognathic System Abnormalities
    - Tooth Abnormalities: 33
      - Anodontia: 374
        Single upper central incisor: 11
Stomatognathic System
- Mouth
  - Dentition
    - Tooth
      - Incisor
        Single upper central incisor: 11

Bernhard C Pseiner Selected Research

Bernhard C Pseiner Research Topics

Disease

Therapy/Procedure