Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding

Abstract

Abstract Heterotaxy syndrome is associated with asplenia/polysplenia and complex congenital heart disease. Facial palsy in heterotaxy is very rare. The management is still challenging with a poor prognosis. Proper counseling to the family about the disease course, treatment modalities, and outcomes is essential.

Keywords

• asplenia
• complex congenital heart disease
• heterotaxy
• situs ambiguous