Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association

 Cornelia de Lange syndrome (CdLS) is a rare non-hereditary syndrome. The key diagnosis is unique facial features, limb anomalies, and growth retardation. Cardiac defects with gastrointestinal and genitourinary anomalies may be associated.

 This is a case of neonatal CdLS that we think is interesting due to its association with a novel congenital heart complex.

 Patients with CdLS have a high incidence of congenital heart disease (CHD), so a cardiologic study of all of these patients is suggested.