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

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 essent...

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Detalles Bibliográficos
Autores principales: Kharel, Sanjeev, Koirala, Dinesh Prasad, Shrestha, Suraj, Sedai, Hari, Shrestha, Bibek Man, Homagain, Sushan, Kandel, Suraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347632/
https://www.ncbi.nlm.nih.gov/pubmed/34401157
http://dx.doi.org/10.1002/ccr3.4573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347632/
https://www.ncbi.nlm.nih.gov/pubmed/34401157
http://dx.doi.org/10.1002/ccr3.4573

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