Cornelia de Lange Syndrome (CdLS) is a rare disease that affects between 1 in 10,000 to 1 in 30,000 newborn babies worldwide. CdLS is caused by mutations in the NIPBL gene in 65% of patients. Less ...

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 ...

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 ...

A team of researchers has discovered a gene for Cornelia de Lange Syndrome, a disorder consisting of mental retardation, heart defects and a number of physical abnormalities. A team of researchers has ...

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 ...

The Cornelia de Lange Syndrome Foundation in Avon has named Marie Concklin-Malloy of Riverton acting executive director. Concklin-Malloy joined the foundation as director of external affairs in 2006 ...

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, ...

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 ...