Conditions / Genetic
amelogenesis imperfecta type 3C
info · Genetic
An amelogenesis imperfecta type 3 that is characterized by hypocalcified enamel in both the primary and secondary dentition and that has_material_basis_in homozygous mutation in the RELT gene on chromosome 11q13.
Signs and symptoms
- Hypocalcification of dental enamel
- Amelogenesis imperfecta
- Anterior open-bite malocclusion
- Yellow-brown discoloration of the teeth
Also known as: AI3C; amelogenesis imperfecta type IIIC; autosomal recessive amelogenesis imperfecta hypocalcification type