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Situs Inversus Totalis in the Neonatal Setting

Situs inversus totalis (SIT) is a rare condition of complete inversion and mirroring of normal human anatomy. The incidence is approximately 1 in 8,000 to 1 in 25,000 live births. SIT is inherited in an autosomal recessive pattern and is associated with multiple gene mutations. It is also commonly s...

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Detalles Bibliográficos
Autores principales: Devera, Jordan, Licandro, Francesca, Ramos, Jean, Taymoorian, Hovik T, Yap, Laurel G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904504/
https://www.ncbi.nlm.nih.gov/pubmed/33654643
http://dx.doi.org/10.7759/cureus.13516