Rare cause of neonatal apnea from congenital central hypoventilation syndrome

Rare cause of neonatal apnea from congenital central hypoventilation syndrome

Abstract 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 h...

Full description

Bibliographic Details
Main Authors: Prakarn Tovichien, Krittin Rattananont, Narathorn Kulthamrongsri, Mongkol Chanvanichtrakool, Buranee Yangthara
Format: Article
Language:English
Published: BMC 2022-02-01
Series:BMC Pediatrics
Subjects:
Case report
cogenital central hypoventilation syndrome
CCHS
neonatal apnea
PHOX2B
Online Access:https://doi.org/10.1186/s12887-022-03167-8

Internet

https://doi.org/10.1186/s12887-022-03167-8

Similar Items