Conditions / Genetic
amelogenesis imperfecta type 2A6
info · Genetic
An amelogenesis imperfecta that is characterized by enamel of normal thickness that is hypomineralized and has a mottled appearance and that has_material_basis_in homozygous mutation in the G protein-coupled receptor-68 (GPR68) on chromosome 14q32.
Signs and symptoms
- Amelogenesis imperfecta
- Enamel hypomineralization
- Anterior open-bite malocclusion
Also known as: Amelogenesis imperfecta, hypomaturation type, IIA6