Amelogenesis imperfecta
ORPHA:88661· ICD-10 K00.5
Definition
A rare genetic odontal or periodontal disorder that represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant, Autosomal recessive, X-linked dominant
- Age of onset
- Infancy, Neonatal