Синдром Трічера-Коллінза
ORPHA:861· ICD-10 Q75.4· Treacher-Collins syndrome
Визначення(English summary)
A rare genetic mandibulofacial dysostosis characterized by bilateral symmetrical oto-mandibular dysplasia including underdeveloped cheekbones (malar hypoplasia), a very small low jaw (micrognathia) and downward-slanting palpebral fissures, coloboma of the lower eyelids, microtia, hearing loss and without abnormalities of the extremities. Intelligence is normal.
- Поширеність
- 1-9 / 1 000 000
- Успадкування
- Autosomal dominant, Autosomal recessive
- Вік початку
- Antenatal, Neonatal