Perioperative outcomes and the effects of anesthesia in congenital central hypoventilation patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Otorhinolaryngology
Link
https://link.springer.com/content/pdf/10.1007/s11325-022-02632-z.pdf
Reference28 articles.
1. Weese-Mayer DE, Berry-Kravis EM, Ceccherini I et al (2010) An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management. Am J Respir Crit Care Med 181:626–644. https://doi.org/10.1164/rccm.200807-1069ST
2. Amiel J, Laudier B, Attié-Bitach T et al (2003) Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 33:459–461. https://doi.org/10.1038/ng1130
3. Silvestri JM, Chen ML, Weese-Mayer DE et al (2002) Idiopathic congenital central hypoventilation syndrome: the next generation. Am J Med Genet 112:46–50. https://doi.org/10.1002/ajmg.10819
4. Matera I, Bachetti T, Puppo F et al (2004) PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome. J Med Genet 41:373–380
5. Paton JY, Swaminathan S, Sargent CW, Keens TG (1989) Hypoxic and hypercapnic ventilatory responses in awake children with congenital central hypoventilation syndrome. Am Rev Respir Dis 140:368–372. https://doi.org/10.1164/ajrccm/140.2.368
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