Conditions / Genetic
amelogenesis imperfecta type 1E
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta that has_material_basis_in X-linked dominant mutation in the gene encoding amelogenin (AMELX).
Signs and symptoms
- Anterior open-bite malocclusion
- Amelogenesis imperfecta
- Enamel hypoplasia
- Abnormal dentin morphology
Also known as: AIH1; X-linked amelogenesis imperfecta 1; X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1; amelogenesis imperfecta hypomaturationtype with snow-capped teeth; amelogenesis imperfecta type IE