Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding
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...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2021-08-01
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| Series: | Clinical Case Reports |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/ccr3.4573 |
| _version_ | 1798036337629069312 |
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| author | Sanjeev Kharel Dinesh Prasad Koirala Suraj Shrestha Hari Sedai Bibek Man Shrestha Sushan Homagain Suraj Kandel |
| author_facet | Sanjeev Kharel Dinesh Prasad Koirala Suraj Shrestha Hari Sedai Bibek Man Shrestha Sushan Homagain Suraj Kandel |
| author_sort | Sanjeev Kharel |
| collection | DOAJ |
| description | 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. |
| first_indexed | 2024-04-11T21:11:28Z |
| format | Article |
| id | doaj.art-da8b7454163347ae97eb049377a02841 |
| institution | Directory Open Access Journal |
| issn | 2050-0904 |
| language | English |
| last_indexed | 2024-04-11T21:11:28Z |
| publishDate | 2021-08-01 |
| publisher | Wiley |
| record_format | Article |
| series | Clinical Case Reports |
| spelling | doaj.art-da8b7454163347ae97eb049377a028412022-12-22T04:03:01ZengWileyClinical Case Reports2050-09042021-08-0198n/an/a10.1002/ccr3.4573Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn findingSanjeev Kharel0Dinesh Prasad Koirala1Suraj Shrestha2Hari Sedai3Bibek Man Shrestha4Sushan Homagain5Suraj Kandel6Institute of Medicine Maharajgunj Medical Campus Kathmandu NepalDepartment of Gastrointestinal and General Surgery Pediatric Surgery Unit Tribhuvan UniversityTeaching Hospital Kathmandu NepalInstitute of Medicine Maharajgunj Medical Campus Kathmandu NepalInstitute of Medicine Maharajgunj Medical Campus Kathmandu NepalInstitute of Medicine Maharajgunj Medical Campus Kathmandu NepalInstitute of Medicine Maharajgunj Medical Campus Kathmandu NepalInstitute of Medicine Maharajgunj Medical Campus Kathmandu NepalAbstract 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.https://doi.org/10.1002/ccr3.4573aspleniacomplex congenital heart diseaseheterotaxysitus ambiguous |
| spellingShingle | Sanjeev Kharel Dinesh Prasad Koirala Suraj Shrestha Hari Sedai Bibek Man Shrestha Sushan Homagain Suraj Kandel Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding Clinical Case Reports asplenia complex congenital heart disease heterotaxy situs ambiguous |
| title | Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding |
| title_full | Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding |
| title_fullStr | Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding |
| title_full_unstemmed | Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding |
| title_short | Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding |
| title_sort | heterotaxy syndrome with complex congenital heart disease facial palsy and asplenia a rare newborn finding |
| topic | asplenia complex congenital heart disease heterotaxy situs ambiguous |
| url | https://doi.org/10.1002/ccr3.4573 |
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