<%@LANGUAGE="JAVASCRIPT"%> Pierre Robin Sequence
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What is Pierre Robin sequence?

  • Pierre Robin sequence is a condition characterized by a wide U-shaped cleft of the palate and a small lower jaw with the tongue positioned toward the back of the mouth. This combination of features can make it difficult or impossible to feed or breathe normally. A baby with Pierre Robin may need special procedures at birth to ensure adequate breathing and feeding.

What special treatment will my child need?

  • The child should be seen shortly after birth by the nurse from the Craniofacial Center to establish adequate feeding and breathing. The child should then be seen for a full team evaluation.
  • If the tongue obstructs the airway or if the child is having any breathing difficulties, he or she will be referred to the pediatric pulmonary clinic. The child may need a lip-tongue plication. This procedure brings the tongue forward by attaching it temporarily to the lower lip, opening the airway so the baby can breathe more freely.
  • An infant with Pierre Robin usually must be bottle-fed (with breast milk or formula) using special nipples. Because of the extra effort to breathe and swallow, many babies require supplemental calories.
  • A hearing test is recommended, and ventilating tubes are usually placed in the ears at the time of palate surgery to reduce the risk of ear infections. Ear infections are more common for a child with a cleft palate.
  • An eye examination is usually recommended as associated eye anomalies are not unusual.
  • Palate surgery will take place around 10 months of age or later if the lower jaw is still retruded.
  • Surgery usually takes about 2-3 hours and the infant remains in the hospital one or two nights.
  • Orthodontic treatment (braces) may or may not be necessary in early adolescence.
  • We expect normal speech after cleft palate repair. In some cases speech therapy is necessary or a second palate surgery is needed.
  • A child with Pierre Robin may encounter social and emotional challenges unique to this condition. Support organizations and resources are available for children and their families (see Support Information).



 

 

 

 

 



 

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