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, ...
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 ...
Purpose: This study reviews prenatal findings in two cases with a suspected diagnosis of Cornelia de Lange Syndrome, a multisystem disorder characterized by somatic defects and mental retardation, ...
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 ...
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 ...
Brannigan’s journey started Aug. 31 in Bar Harbor, Maine, and he should reach Worcester Tuesday. The day before his arrival in Worcester, Brannigan will touch down in Framingham. And the day after ...
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 ...
Those suffering from heart ailments can turn to the American Heart Association for help. The American Cancer Society aids people and families battling that life-threatening disease. So where do you ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results