<%@LANGUAGE="JAVASCRIPT"%> Cleft Lip and Palate
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The following is a list of expectations for a child born with a cleft lip and palate. Although each child is unique, this is intended to give a general idea of what to expect:

  • An infant with cleft lip and palate usually must be bottle-fed (with breast milk or formula) using special nipples.
  • Soon after birth and in preparation for surgery, the lip may need to be taped to help reduce the width of the cleft.
  • A hearing test is recommended , and ventilating tubes are usually placed in the ears at the time of lip 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 because associated eye anomalies are not unusual.
  • Lip surgery will take place around 10 weeks of age (or 10 lbs).
  • Lip surgery takes about 2-3 hours and the infant usually remains in the hospital one night.
  • Palate surgery will take place around 10 months of age or when a child begins to make sounds of speech.
  • Palate surgery usually takes about 2-3 hours and the infant remains in the hospital one or two nights.
  • Orthodontic treatment (braces) and/or alveolar bone grafting (filling the remaining gap in the gum line) will usually be necessary. The first phase of treatment is usually the widening of the upper jaw with an orthodontic appliance when the permanent front teeth come in, at about seven years of age. The bone grafting surgery is done after the widening.
  • 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 a cleft lip and palate 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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