Heterotaxy syndrome with complex congenital heart disease,facial palsy,and asplenia: A rare newborn finding |
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Authors: | Sanjeev Kharel Dinesh Prasad Koirala Suraj Shrestha Hari Sedai Bibek Man Shrestha Sushan Homagain Suraj Kandel |
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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 |
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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. |
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Keywords: | asplenia complex congenital heart disease heterotaxy situs ambiguous |
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