CdLS (Cornelia de Lange Syndrome) is a rare genetic disorder that affects about 1 in every 10,000 babies born in the US. This disorder can cause a range of symptoms, including physical, medical, and ...

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 ...

Alma, 4 ans, bénéficiera de la Bûche de la générosité organisée samedi 14 décembre à Crest. Sa famille, qui habite Bourg-de-Péage, souhaite financer un stage en Autriche pour donner toutes les chances ...

Apporter aide et soutien aux enfants en situation de handicap et proposer un moment de répit aux mamans, telle est la mission que s’est donnée l’association On est ensemble. Rencontre avec la ...

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 condition that can affect multiple organs. CdLS may cause various symptoms, including intellectual disability and characteristic facial features.