Pierre Robin sequence (PRS) consists of the clinical triad of congenital micrognathia,
glossoptosis, and airway obstruction with variable inclusion of a cleft palate (Fig. 1). When …

Pierre Robin syndrome (PRS) is characterized of a triad of clinical signs: micrognathia,
glossoptosis and obstruction of the upper airways frequently associated with palatal cleft. It …

Pierre Robin sequence is defined by the clinical triad: mandibular hypoplasia, glossoptosis,
and airway obstruction. In his 1923 publication, Robin first described the eponymous …

Objective To provide recommendations for the comprehensive management of airway
obstruction in patients with Robin Sequence. Methods Expert opinion by the members of the …

Objectives: Summarize the etiology of Pierre Robin sequence. Describe the classic physical
exam findings associated with Pierre Robin sequence. Outline the treatment considerations …

Background: Pierre Robin Sequence (PRS) is characterized by micrognathia, glossoptosis,
cleft palate, and airway distress. The aims of initial treatment are the improvement of airway …

Background Robin sequence (RS) is a congenital disorder characterized by cleft palate,
micrognathia, and glossoptosis which can result in clinically significant upper airway …

Objectives: This retrospective cohort study uses endoscopic assessment of the pharyngeal
phase of swallowing in infants with laryngomalacia, to ascertain the impact of infant …

Objective: Mandibular distraction osteogenesis (MDO) is frequently performed to address
airway obstruction in patients with Pierre Robin sequence (PRS), though more recently the …

Background: Robin sequence is defined by the clinical triad of micrognathia, glossoptosis,
and upper airway obstruction, and is frequently associated with cleft palate and failure to …