Conditions / Genetic
amelogenesis imperfecta type 3B
info · Genetic
An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene.
Signs and symptoms
- Amelogenesis imperfecta
- Enamel hypomineralization