Multidisciplinary approach to congenital central hypoventilation syndrome during pregnancy: case report

Congenital central hypoventilation syndrome is a rare genetic disorder that affects control of breathing caused by variants in the paired-like homeobox 2B (PHOX2B) gene. During pregnancy, women with congenital central hypoventilation syndrome are at risk for hypoventilation and require frequent asse...

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Detalles Bibliográficos
Autores principales: Akingbola, Akinbolaji, Kasi, Ajay S., Yamamura, Yasuko, Pusalavidyasagar, Snigdha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491849/
https://www.ncbi.nlm.nih.gov/pubmed/37692770
http://dx.doi.org/10.1016/j.xagr.2023.100263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491849/
https://www.ncbi.nlm.nih.gov/pubmed/37692770
http://dx.doi.org/10.1016/j.xagr.2023.100263

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