Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding
2021
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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