Results 181 to 190 of about 3,814,939 (217)
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2006
The Pierre Robin sequence will show hypoplasia of the mandible (micrognathia cleft palate/glossoptosis) causing retraction of the sternum synopsis and malnutrition. This study will show cephalometric changes that can occur over time. There are a number of surgical or nonsurgical procedures that can be utilized during the early neonatal period that can ...
Samuel Pruzansky, Julius B. Richmond
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The Pierre Robin sequence will show hypoplasia of the mandible (micrognathia cleft palate/glossoptosis) causing retraction of the sternum synopsis and malnutrition. This study will show cephalometric changes that can occur over time. There are a number of surgical or nonsurgical procedures that can be utilized during the early neonatal period that can ...
Samuel Pruzansky, Julius B. Richmond
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Pierre Robin Sequence/Pierre Robin malformation
Asian Journal of Nursing Education and Research, 2016Pierre robin sequence (PRS) is a rare condition characterized by cleft palate, retrognathia and glossoptosis, PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next. The reported birth prevalence of PRS ranges from 1 in 2000 to 1 in 30, 000, Bush and Williams suggested 1 in 8500.
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2021
Pierre Robin sequence (PRS, or “Robin sequence, RS) is a clinical entity characterized by the triad of mandibular hypoplasia (small jaw), glossoptosis (hypotonic, retracted tongue), and respiratory obstruction. In addition, about half of patients have a posterior cleft palate [1] (Fig. 25.1).
Krishna Shama Rao, Chetana Kumar
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Pierre Robin sequence (PRS, or “Robin sequence, RS) is a clinical entity characterized by the triad of mandibular hypoplasia (small jaw), glossoptosis (hypotonic, retracted tongue), and respiratory obstruction. In addition, about half of patients have a posterior cleft palate [1] (Fig. 25.1).
Krishna Shama Rao, Chetana Kumar
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2018
Pierre Robin Sequence (PRS) is a rare condition described in the early twentieth century as the triad of micrognathia, glossoptosis and upper airway obstruction occurring in infants.Up to 90% of infants affected will have a cleft palate.The severity of the condition varies widely.The airway obstruction may be immediately life threatening, or associated
Fallon R. Brewer, Lorie M. Harper
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Pierre Robin Sequence (PRS) is a rare condition described in the early twentieth century as the triad of micrognathia, glossoptosis and upper airway obstruction occurring in infants.Up to 90% of infants affected will have a cleft palate.The severity of the condition varies widely.The airway obstruction may be immediately life threatening, or associated
Fallon R. Brewer, Lorie M. Harper
+4 more sources
Airway management in Pierre Robin sequence☆☆☆★
Otolaryngology - Head and Neck Surgery, 1998There is a great deal of controversy regarding the long‐term management of airway obstruction in children with Pierre Robin sequence. All 23 pediatric otolaryngology fellowship programs were surveyed to determine their current practice patterns. Issues that were addressed included methods of evaluation of airway obstruction, including polysomnography ...
C M, Myer +4 more
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A New Grading of Pierre Robin Sequence
The Cleft Palate Craniofacial Journal, 2008Objective: Pierre Robin sequence (PRS) involves the triad of micrognathia, glossoptosis, and cleft palate. Neonates with PRS suffer from two problems—airway obstruction and feeding difficulties—but the severity of these problems varies greatly.
Annie, Cole +2 more
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Educational achievements in Pierre Robin Sequence
Journal of Plastic Surgery and Hand Surgery, 2012The aim of this retrospective population-based study was to determine if there is any significant difference in academic achievement between students with a Pierre Robin Sequence (PRS) compared with the general population of Swedish students at the typical time of graduation from compulsory school (usually at 16 years of age).
Persson, Martin +4 more
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Aicardi syndrome with Pierre Robin sequence
Journal of American Association for Pediatric Ophthalmology and Strabismus, 2004i f f p E p v s I x c F M U s icardi syndrome was first described in 1965 by a rench neurologist as a tetrad of infantile spasms, genesis of the corpus callosum, chorioretinal lacunae, nd mental retardation. This syndrome is believed to e caused by an X-linked dominant gene that is lethal n hemizygous males. Other associated anomalies, ncluding ectopic
Allison A, Jensen +1 more
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Surgical Considerations in Pierre Robin Sequence
Clinics in Plastic Surgery, 2014The neonatal morbidity and mortality associated with Pierre Robin sequence has decreased with improved nonsurgical and surgical methods for airway protection. With the introduction of distraction osteogenesis and the understanding that improved outcomes occur with a systematic approach to patient management that includes mandibular distraction for ...
Justine C, Lee, James P, Bradley
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