The Pierre Robin Syndrome

JAMA ◽  
1963 ◽  
Vol 184 (9) ◽  
pp. 191
2017 ◽  
Vol 71 (2) ◽  
pp. 141
Author(s):  
Ramush Bejiqi ◽  
Ragip Retkoceri ◽  
Hana XhemaBejiqi ◽  
Rinor Bejiqi ◽  
Arlinda Maloku

2020 ◽  
Author(s):  
Yanli Liu ◽  
Jiashuo Wang ◽  
Shan Zhong

Abstract Background: Difficult tracheal intubation is a problem commonly encountered by anesthesiologists in the clinic. Methods: In this retrospective study, case-level clinical data and computed tomography images of 96 infants with Pierre-Robin syndrome were included in the analysis. First, computed tomography images were labeled by a clinically experienced physician. Then color space conversion, binarization, contour acquisition, and area calculation processing were performed on the annotated files. Finally, we calculated the correlation coefficient between the seven clinical factors and tracheal intubation difficulty, and the difference in each risk factor under tracheal intubation difficulty. Results: The absolute value of the correlation coefficient between throat area and tracheal intubation difficulty is 0.54, and the difference of throat area under tracheal intubation difficulty is significant. Body surface area, weight and gender also show significant difference under tracheal intubation difficulty. Conclusions: There is a significant correlation between throat area and tracheal intubation difficulty in infants with Pierre-Robin syndrome. Body surface area, weight and gender may have an impact on tracheal intubation difficulty in infants with Pierre-Robin syndrome.


1980 ◽  
Vol 33 (2) ◽  
pp. 237-241 ◽  
Author(s):  
D.O. Maisels ◽  
J.H. Stilwell

PEDIATRICS ◽  
1965 ◽  
Vol 36 (3) ◽  
pp. 336-341 ◽  
Author(s):  
Wallace M. Dennison

The whole object of the medical and nursing care of infants with the Pierre Robin syndrome is to keep them alive and thriving in their perilous passage through the early months of life until the failure of mandibular development in utero is subsequently rectified by nature. From my limited experience of this condition I suggest that surgery has little to offer in the treatment of the Pierre Robin syndrome. Cap suspension, tube feeding, and skilled nursing are more important than any surgical procedures.


PEDIATRICS ◽  
1962 ◽  
Vol 30 (3) ◽  
pp. 450-458
Author(s):  
Marvin H. Goldberg ◽  
Roger H. Eckblom

The diagnosis of the Pierre Robin Syndrome, cleft palate, micrognathia, and golssoptosis is re-emphasized. The clinical symptoms are discussed. The treatments advocated in the literature are described. A simple traction device, employing a horizontal suture through the mid-body of the tongue and an elastic traction system, is explained. Five cases of the syndrome are reported. In one the condition was mild; in the other four the tongue traction device was employed. In one sick infant with a congenital heart disease a tracheotomy had to be performed. Much difficulty was experienced following this, and the operation is only recommended when traction alone does not control the handling of the profusion of mucus and bouts of apnea. A removable acrylic palatine obturator was used as an adjunct to nipple feedings in three patients, with excellent results. The method of production of this "false palate" is described.


1976 ◽  
Vol 86 (7) ◽  
pp. 979-983 ◽  
Author(s):  
Abraham Lapidot ◽  
Firooz Rezvani ◽  
Dessalegn Terrefe ◽  
Nahum Ben-Hur

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