amelogenesis imperfecta type 1H

info · Genetic · ICD-10: K00.5

An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the integrin beta-6 gene (ITGB6) on chromosome 2q24.

Signs and symptoms

Anterior open-bite malocclusion
Amelogenesis imperfecta
Enamel hypoplasia
Yellow-brown discoloration of the teeth
Dental enamel pits

Also known as: AI1H; amelogenesis imperfecta type IH