Conditions / Genetic
solitary median maxillary central incisor
info ยท Genetic
A tooth disease characterized by single deciduous and parmanent maxillary central incisor that may be isolated or occur with a range of other systemic anomalies that has_material_basis_in heterozygous mutation in SHH on chromosome 7q36.3.
Signs and symptoms
- Prominent median palatal raphe
- Decreased response to growth hormone stimulation test
- Midnasal stenosis
- Choanal atresia
- Hypotelorism
- Holoprosencephaly
- Pyriform aperture stenosis
- Short stature
- Torus palatinus
- Specific learning disability
Also known as: SMMCI; fused incisors; single central maxillary incisor; single median maxillary central incisor; single upper central incisor