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