Impact of Cleft Palate on Tongue-Based Upper Airway Obstruction in Pierre Robin Sequence

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Hannes Prescher ◽  
Jill R. Froimson ◽  
Pranav N. Haravu ◽  
Russell R. Reid
Author(s):  
Alessandro Amaddeo ◽  
Veronique Abadie ◽  
Veronique Soupre ◽  
Christel Chalouhi ◽  
Marta Fernandez Bolanos ◽  
...  

2007 ◽  
Vol 151 (2) ◽  
pp. 145-149 ◽  
Author(s):  
Wolfgang Buchenau ◽  
Michael S. Urschitz ◽  
Judit Sautermeister ◽  
Margit Bacher ◽  
Tina Herberts ◽  
...  

1992 ◽  
Vol 29 (3) ◽  
pp. 205-209 ◽  
Author(s):  
Robert J. Shprintzen

“Pierre Robin” is one of the most readily recognized diagnostic eponyms in medicine, yet it is a poorly understood nonspecific grouping of malformations that has no prognostic significance. Although the science of dysmorphology and in particular those who study children with clefts would be reluctant to forego the use of this diagnosis, the reality is that fewer than 20 percent of children with micrognathia and cleft palate should have this term applied. The syndromic diagnoses of 100 children with Robin sequence are presented and discussed in relation to morphologic characteristics. Upper airway obstruction and Its relationship to feeding problems is also discussed.


1997 ◽  
Vol 111 (12) ◽  
pp. 1155-1156 ◽  
Author(s):  
A. P. Bath ◽  
P. D. Bull

AbstractPierre Robin sequence (PRS) presents in the neonatal period with upper airway obstruction and feeding difficulties. Infants with pronounced micrognathia may fail to thrive because of chronic airway obstruction, or experience severe respiratory distress. This is potentially fatal and surgical intervention in these cases is necessary. We present our series of cases with severe PRS requiring surgical relief of their airway obstruction, and the reasons for preferring tracheostomy over glossopexy.


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