Conditions / Genetic
amelogenesis imperfecta hypomaturation type 2A3
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.
Signs and symptoms
- Hypomature dental enamel
- Amelogenesis imperfecta
- Enamel hypomineralization
Also known as: AI2A3; amelogenesis imperfecta hypomaturation type IIA3; amelogenesis imperfecta type IIA3