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...

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Bibliografiska uppgifter

Huvudupphov:	Prakarn Tovichien, Krittin Rattananont, Narathorn Kulthamrongsri, Mongkol Chanvanichtrakool, Buranee Yangthara
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	BMC 2022-02-01
Serie:	BMC Pediatrics
Ämnen:	Case report cogenital central hypoventilation syndrome CCHS neonatal apnea PHOX2B
Länkar:	https://doi.org/10.1186/s12887-022-03167-8
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