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Heterotaxy syndrome with complex congenital heart disease,facial palsy,and asplenia: A rare newborn finding
Authors:Sanjeev Kharel  Dinesh Prasad Koirala  Suraj Shrestha  Hari Sedai  Bibek Man Shrestha  Sushan Homagain  Suraj Kandel
Affiliation:1. Institute of Medicine, Maharajgunj Medical Campus, Kathmandu Nepal ; 2. Department of Gastrointestinal and General Surgery, Pediatric Surgery Unit, Tribhuvan University, Teaching Hospital, Kathmandu Nepal
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
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