Синдром камптодактилії - контрактури суглобів - дефектів лицьового скелета
ORPHA:1323· ICD-10 Q87.0· Camptodactyly-joint contractures-facial skeletal defects syndrome
Визначення(English summary)
A rare multiple congenital anomalies syndrome characterized by the association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline).
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant, Autosomal recessive
- Вік початку
- Neonatal