Cornelia de Lange syndrome
ORPHA:199· ICD-10 Q87.1
Definition
A rare multiple congenital anomalies syndrome characterized by facial dysmorphism, hypertrichosis, mild to profound intellectual disability, intrauterine growth restriction (IUGR) and/or postnatal growth restriction, feeding difficulties, abnormalities of the hands and feet (ranging from severe reductional limb abnormalities, oligodactyly, to brachymetacarpia of the first metacarpus). Variable visceral malformations may be present.
- Prevalence
- 1-9 / 100 000
- Inheritance
- Autosomal dominant, Not applicable, X-linked recessive
- Age of onset
- Antenatal, Neonatal