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 (typus degenerativus amstelodamensis, CdLS, Brachmann syndrome) is a complex, congenital, multi-gene anomaly characterized by mental retardation. Its features include growth ...

International Cornelia de Lange Syndrome (CdLS) Awareness Day 2024: From date to significance, here's all that you need to know about this important day. International Cornelia de Lange Syndrome (CdLS ...

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 ...

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, ...

Mom Marcia Knowles is rallying a "Hoof It 4 Hunter" walk-a-thon to raise awareness for Cornelia de Lange Syndrome, a condition she knew nothing about until her own son was diagnosed. Hunter James ...

International CdLS Awareness Day, observed annually on the second Saturday of May, is a momentous occasion dedicated to raising awareness about Cornelia de Lange Syndrome (CdLS), a rare genetic ...

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 ...