Pierre Robin Syndrome (Pierre Robin Sequence) - Cleveland Clinic
Pierre Robin syndrome (PRS), or Pierre Robin sequence, is a rare birth defect that happens during fetal development. It’s a group of conditions that affect your baby’s jaw and mouth so it may be hard for them to breathe, nurse or feed from a bottle.
Pierre Robin Sequence - Johns Hopkins Medicine
Pierre Robin sequence is also known as Pierre Robin syndrome or Pierre Robin malformation. It is a rare congenital birth defect characterized by an underdeveloped jaw, backward displacement of the tongue and upper airway obstruction.
Pierre Robin Syndrome - StatPearls - NCBI Bookshelf
2023年8月7日 · Pierre Robin sequence is a constellation of micrognathia, glossoptosis, and upper airway obstruction. It is a clinical diagnosis that can range in severity and may be associated with genetic syndromes.
Pierre Robin sequence - Wikipedia
Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities. The three main features are micrognathia (abnormally small mandible ), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing ...
Pierre Robin Sequence - Symptoms, Causes, Treatment | NORD
2018年8月6日 · Pierre Robin sequence (PRS) is characterized by a small lower jaw (micrognathia) and displacement of the tongue toward the back of the oral cavity (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate).
Pierre Robin Syndrome: Symptoms, Treatment, Life Expectancy
2024年12月9日 · Learn about Pierre Robin syndrome (aka Pierre Robin sequence) and how it can affect a baby’s breathing, feeding, hearing, and development.
Pierre Robin Sequence | Causes, Symptoms, Diagnosis & Treatment
What is Pierre Robin Sequence? Pierre Robin sequence is a set of abnormalities in a baby that develops during pregnancy. It is called a sequence because one of its features − an undeveloped lower jaw − starts off a sequence of other malformations while a baby is developing in utero.
Pierre Robin Syndrome - Children's Hospital of Philadelphia
What is Pierre Robin syndrome? Pierre Robin syndrome is a congenital condition recently linked to genetic anomalies at chromosomes 2, 11 or 17. Often called Pierre Robin sequence, the disease is a chain of developmental malformations, each leading to the next.
Isolated Pierre Robin sequence - MedlinePlus
Pierre Robin sequence is a set of abnormalities affecting the head and face, consisting of a small lower jaw (micrognathia), a tongue that is placed further back than normal (glossoptosis), and blockage (obstruction) of the airways. Most people with Pierre Robin sequence are also born with an opening in the roof of the mouth (a cleft palate).
Pierre Robin Sequence (PRS) (for Parents) - KidsHealth
What Is Pierre Robin Sequence (PRS)? Babies born with Pierre Robin sequence (PRS) have a jaw that's smaller than normal. A jaw that’s too small can push the tongue farther back in the mouth than usual. That blocks the baby’s airway, causing breathing trouble.
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