Cornelia de Lange syndrome (CdLS) is a rare genetic disorder with symptoms, including facial anomalies (such as fused eyebrows, short nose, upturned nose tip, and downturned mouth corners), growth ...

Cornelia de Lange syndrome (CdLS) presentation involves craniofacial anomalies. Mutations in seven genes have been associated with CdLS. However, the clinical presentation and mutational profiles of ...

An international team of researchers has discovered the gene for Cornelia de Lange syndrome, a disabling, multisystem genetic disease that affects an estimated one in 10,000 children. The finding is ...

British Army Maj. Chris Brannigan said he will take any step necessary to raise awareness about the relatively unknown genetic condition, Cornelia de Lange syndrome, from which his 9-year-old daughter ...