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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