Синдром камптодактилії - гіперплазії фіброзної тканини - скелетних аномалій
ORPHA:1321· ICD-10 Q87.2· Camptodactyly-fibrous tissue hyperplasia-skeletal anomalies syndrome
Визначення(English summary)
An extremely rare chondrodysplastic malformation syndrome characterized by the combination of arachnodactyly, becoming evident at around the age of 10, camptodactyly, and scoliosis. Additional reported manifestations include a mild intellectual disability and a mild facial dysmorphism including a broad nose and flaring nostrils. There have been no further descriptions in the literature since 1972.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Neonatal