Literature DB >> 1554454

Upper airway function in Ondine's curse.

T S Olson1, G E Woodson, G P Heldt.   

Abstract

Congenital central alveolar hypoventilation (Ondine's curse) is a rare disorder with absence of automatic control of ventilation but preservation of voluntary breathing. Phrenic pacing, used to treat this condition, is usually not successful without a tracheotomy. We performed fiberoptic videoendoscopy on an affected infant airway. During wakefulness and ventilation by a negative pressure ventilator, the airway was normal, but with sleep onset, passive inspiration produced phasic epiglottic collapse. This case demonstrates the importance of central control in maintaining upper airway patency.

Entities:  

Mesh:

Year:  1992        PMID: 1554454     DOI: 10.1001/archotol.1992.01880030098020

Source DB:  PubMed          Journal:  Arch Otolaryngol Head Neck Surg        ISSN: 0886-4470


  4 in total

1.  Airway obstruction in congenital central hypoventilation syndrome.

Authors:  Alexandra K Reverdin; Ricardo Mosquera; Giuseppe N Colasurdo; Cindy K Jon; Roya M Clements
Journal:  BMJ Case Rep       Date:  2014-05-19

2.  Epiglottic movements during breathing in humans.

Authors:  T C Amis; N O'Neill; E D Somma; J R Wheatley
Journal:  J Physiol       Date:  1998-10-01       Impact factor: 5.182

3.  Negative extrathoracic pressure ventilation in central hypoventilation syndrome.

Authors:  H Hartmann; M H Jawad; J Noyes; M P Samuels; D P Southall
Journal:  Arch Dis Child       Date:  1994-05       Impact factor: 3.791

4.  Central Hypoventilation: A Rare Complication of Wallenberg Syndrome.

Authors:  Keithan Sivakumar; Manveer Garcha; Dev Mehta; Megan C Leary; Hussam A Yacoub
Journal:  Case Rep Neurol Med       Date:  2018-03-21
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.