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Aug 7, 2023 · Introduction. Pierre Robin sequence (PRS) is characterized by the clinical triad of micrognathia (mandibular hypoplasia), glossoptosis (downward displacement of the tongue), and upper airway obstruction.
- Diana Baxter, Anthony L. Shanks
- 2023/08/07
- 2021
Pierre Robin sequence [a] ( / pjɛərrɔːˈbæ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.
May 29, 2024 · Pierre Robin syndrome is a rare birth defect that affects the jaw, mouth and breathing. Learn about the diagnosis, complications and management of this condition from Cleveland Clinic experts.
Pierre Robin sequence is a set of abnormalities in a baby that develops during pregnancy, including a small lower jaw, tongue obstruction and cleft palate. Learn about the causes, symptoms, diagnosis and treatment options from Cincinnati Children's experts.
Learn about Pierre Robin sequence, a rare congenital birth defect that affects the jaw, tongue, palate and airway. Find out the causes, symptoms, diagnosis and treatment options for this condition.
Learn about the causes, diagnosis and treatment of Pierre Robin syndrome, a genetic condition that affects the lower jaw, tongue and airway. Find out how CHOP can provide coordinated care and support for children with this condition.
Pierre Robin ( Pee-air Roe-bahn) sequence, also called Pierre Robin syndrome, or PRS, is a condition where babies are born with a small lower jaw, have difficulties breathing (airway obstruction) and often (but not always) have a cleft of the palate (an opening in the roof of the mouth).
