What is Cornelia de Lange Syndrome? Cornelia de Lange syndrome is a developmental disorder that can affect multiple body parts. Although the exact prevalence of Cornelia de Lange syndrome is unknown, ...

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 ...

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 ...

PORTSMOUTH — May 11 is awareness day for Cornelia de Lange syndrome, a rare genetic disorder. The Lyons family of Portsmouth knows all about it. Their son Luke, now 11, was born with CdLS, which has ...

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 ...

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 ...

PORTSMOUTH — May 11 is awareness day for Cornelia de Lange syndrome, a rare genetic disorder. The Lyons family of Portsmouth knows all about it. Their son Luke, now 11, was born with CdLS, which has ...