Rare cause of neonatal apnea from congenital central hypoventilation syndrome

BACKGROUND: Congenital central hypoventilation syndrome (CCHS) is a rare condition caused by mutations in the Paired-Like Homeobox 2B (PHOX2B) gene. It causes alveolar hypoventilation and autonomic dysregulation. This report aimed to raise awareness of this rare cause of neonatal apnea and hypoventi...

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Detalles Bibliográficos
Autores principales: Tovichien, Prakarn, Rattananont, Krittin, Kulthamrongsri, Narathorn, Chanvanichtrakool, Mongkol, Yangthara, Buranee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867765/
https://www.ncbi.nlm.nih.gov/pubmed/35209861
http://dx.doi.org/10.1186/s12887-022-03167-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867765/
https://www.ncbi.nlm.nih.gov/pubmed/35209861
http://dx.doi.org/10.1186/s12887-022-03167-8

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