Penn State Children's Hospital
Calendar  I  Contact Us  I  Help  I  Search
 
  1-800-243-1455
 

 

 

Health & Disease Information

 
 

A   B   C   D   E   F   G   H   I   J   K   L   M   N   O   P  Q   R   S   T   U   V   W   X   Y   Z

 
 

Cleft Palate/Cleft Lip

What is it?

A cleft is a birth defect that occurs when the tissues of a fetus's lip and/or palate do not properly fuse very early in pregnancy. A cleft palate is a condition in which the roof of the mouth abnormally opens into the floor of the nose. A cleft lip is an elongated opening between the upper lip and the nose. It may involve one or both sides of the lip and may occur with or without a cleft palate.

Who gets it?

Cleft palate and cleft lip are conditions present at birth. Cleft palate occurs approximately once in every 2,500 live births and affects females more than males. However, twice as many boys as girls are afflicted with a cleft lip, both with and without a cleft palate. Clefting occurs most often in Asians, Latinos, and Native Americans (1 of 500 births) and least often in people of African descent (1 of 1000 births).

What causes it?

Cleft palate and cleft lip can be caused by either genetic or environmental factors. The genes that cause clefting may be passed from either parent. Environmental factors include the mother's diet, use of drugs or tobacco, and the rubella virus.

What are the symptoms?

Babies born with cleft lips or cleft palates may have trouble breathing, as well as swallowing. They cannot adequately suck, so they cannot nurse and must be fed with a special bottle or a bulbar syringe. Later, when their teeth erupt, the upper and lower teeth and jaws are often misaligned, resulting in difficulty chewing. A cleft palate also affects a child's speech since the palate is necessary for speech formation. Children with clefts are also vulnerable to frequent ear infections. Their Eustachian tubes do not effectively drain fluid from the middle ear to the mouth, so fluid accumulates, pressure builds, and infection sets in.

How is it diagnosed?

Clefting is apparent upon examination immediately after birth.

What is the treatment?

Cleft lip defects may be repaired shortly after birth, but many doctors prefer to operate on infants according to the "rule of 10"- when the child is at least 10 weeks old and weighs at least 10 pounds. While repair of the cleft lip is usually successful in one operation, a second operation may be performed later to refine the scar. Cleft palates are repaired after the first or second year of life with a series of operations. If the defect lies primarily in the forward, bony portion of the palate (called the "hard palate"), doctors may wait to operate until the child is between five and seven years old and has more bone growth. One option for nonsurgical treatment is a prosthetic appliance worn as an artificial palate. Later, the child will need orthodontic treatment to realign the structures of the mouth for proper function. Children with frequent ear infections may need to have drainage tubes inserted into their ears to prevent hearing loss.

Reconstructive surgery, orthodontic treatment, and speech therapy can minimize the effects of clefting. Breathing, eating, and speech are also greatly improved with treatment, so a child born with a cleft lip and/or palate may lead a normal life.


This information has been designed as a comprehensive and quick reference guide written by our health care reviewers.  The health information written by our authors is intended to be a supplement to the care provided by your physician.  It is not intended nor implied to be a substitute for professional medical advice.

Back

 
   



Penn State Milton S. Hershey Medical Center ©2004
This page was last updated on January 03, 2007
Contact Us