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What is ‘Pierre Robin sequence’?
Journal of Plastic, Reconstructive and Aesthetic Surgery, 2009Different nosology has hampered our understanding of patients with Robin sequence. Defining this disorder correctly has important consequences for physicians and parents. While reviewing treatment options for Robin sequence we were surprised to see how often different definitions were used to describe this condition.
A B Mink van der Molen
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Management of Infants with Pierre Robin Sequence
Cleft Palate-Craniofacial Journal, 2003Objective Several methods of treating babies with Pierre Robin sequence have been described since the condition itself was first documented in 1923. The main aim of treatment has been to relieve upper airway obstruction. Treatment methods used range from positioning of the baby to invasive surgery.
Silke, Wagener +4 more
exaly +3 more sources
The prenatal diagnosis of Pierre-Robin sequence
Prenatal Diagnosis, 1999The purpose of this study was to evaluate the spectrum of prenatal sonographic and chromosomal findings, associated anomalies and perinatal and neonatal outcomes in cases with Pierre-Robin sequence. All cases (20) with Pierre Robin sequence, who were born at China Medical College Hospital between 1990 and 1997, were included and analysed in this series.
Y Y, Hsieh +5 more
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Glossoptosis in Pierre Robin sequence
Archives of Disease in Childhood, 2018A newborn baby presented with cleft palate in association with Pierre Robin sequence, a triad of micrognathia, cleft palate (typically U-shaped rather than V-shaped) and glossoptosis. Initial airway management required temporary nasogastric feeding and placement of a nasopharyngeal airway.
Kevin C, Cahill, David J A, Orr
openaire +2 more sources
Survey of Anesthesiology, 2014
The clinical triad of micrognathia (small mandible), glossoptosis (backward, downward displacement of the tongue), and airway obstruction defines the Pierre Robin sequence (PRS). Airway obstruction and respiratory distress are clinical hallmarks. Patients may present with stridor, retractions, and cyanosis.
Franklyn, Cladis +5 more
openaire +2 more sources
The clinical triad of micrognathia (small mandible), glossoptosis (backward, downward displacement of the tongue), and airway obstruction defines the Pierre Robin sequence (PRS). Airway obstruction and respiratory distress are clinical hallmarks. Patients may present with stridor, retractions, and cyanosis.
Franklyn, Cladis +5 more
openaire +2 more sources
Neonatal Network, 1999
The labelPierre Robin sequenceis given to infants presenting with a triad of specific congenital anomalies: micrognathia, glossoptosis, and cleft palate. However, this label should be considered the first, not the final, step in the diagnostic process. In approximately 80 percent of newborns with Pierre Robin sequence, the triad of anomalies is part of
C A, Prows, P L, Bender
openaire +2 more sources
The labelPierre Robin sequenceis given to infants presenting with a triad of specific congenital anomalies: micrognathia, glossoptosis, and cleft palate. However, this label should be considered the first, not the final, step in the diagnostic process. In approximately 80 percent of newborns with Pierre Robin sequence, the triad of anomalies is part of
C A, Prows, P L, Bender
openaire +2 more sources