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Congenital central hypoventilation syndrome: diagnostic and management challenges
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder with failure of central control of breathing and of the autonomic nervous system function due to a mutation in the paired-like homeobox 2B (PHOX2B) gene. Affected patients have absent or negligible ventilatory sensitivity...
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| Publicado no: | Pediatric Health Med Ther |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5683295/ https://ncbi.nlm.nih.gov/pubmed/29388615 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PHMT.S95054 |
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