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

Introduction: Cornelia de Lange syndrome (CdLS) is a rare non-hereditary syndrome. The key diagnosis unique facial features, limb anomalies, and growth retardation. Cardiac defects with gastrointestinal genitourinary anomalies may be associated. Case Presentation: This case of neonatal CdLS that we think interesting due to its association novel congenital heart complex. Conclusions: Patients have high incidence disease (CHD), so cardiologic study all these patients suggested.