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Mar 19, 2024 · Pierre Robin sequence (or syndrome) is a rare congenital condition that results in a combination of problems present at birth. These problems include an underdeveloped lower jaw, cleft palate, a tongue that is placed very far back in the throat, and airway obstruction.
May 8, 2024 · Pierre Robin Syndrome is a congenital condition characterised by: small lower underdeveoloped jaw (micrognathia) cleft palate (when a baby is born with an opening (a cleft) in the roof of the mouth, leaving a hole between the nose and the mouth) displacement of the tongue towards the back of the throat (glossoptosis).
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Sep 8, 2022 · Pierre Robin sequence (PRS; also referred to as Pierre Robin malformation, Pierre Robin malformation sequence, Robin sequence, Pierre Robin syndrome, and Pierre Robin anomalad) is a condition consisting of three essential components [ 1, 2] : Micrognathia or retrognathia. Cleft palate (usually U-shaped but sometimes V-shaped)
Pierre Robin sequence, also known as Pierre Robin complex or syndrome, is a birth defect characterized by a wide, U-shaped cleft palate, a small lower jaw and a tongue that tends to fall back toward the throat, potentially obstructing the airway. Because this combination of features can make it difficult or impossible for a baby with Pierre ...
Pierre Robin syndrome (PRS), also called Pierre Robin sequence, is a congenital condition characterized by a smaller-than-normal lower jaw, a tongue that falls back in the throat and airway obstruction. In many cases, children with PRS will also have cleft palate.
Pierre Robin Sequence and Syndrome (PRS) is a complex condition which can exist on its own or in conjunction with many other genetic and/or syndromic conditions. Currently, there is no genetic test to determine the cause for PRS. Statistics suggest that approximately 65% of children diagnosed with PRS are reported to have coexisting syndromes.
