Congenital Central Hypoventilation Syndrome: Optimizing Care with a Multidisciplinary Approach

Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder affecting respiratory control and autonomic nervous system function caused by variants in the paired-like homeobox 2B (PHOX2B) gene. Although most patients are diagnosed in the newborn period, an increasing number of patie...

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Detalles Bibliográficos
Autores principales: Kasi, Ajay S, Li, Hong, Harford, Kelli-Lee, Lam, Humphrey V, Mao, Chad, Landry, April M, Mitchell, Sarah G, Clifton, Matthew S, Leu, Roberta M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963195/
https://www.ncbi.nlm.nih.gov/pubmed/35360554
http://dx.doi.org/10.2147/JMDH.S284782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963195/
https://www.ncbi.nlm.nih.gov/pubmed/35360554
http://dx.doi.org/10.2147/JMDH.S284782

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