Недосконалий амелогенез
ORPHA:88661· ICD-10 K00.5· Amelogenesis imperfecta
Визначення(English summary)
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.
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant, Autosomal recessive, X-linked dominant
- Вік початку
- Infancy, Neonatal