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Pediatric Cleft Palate

A cleft palate is a gap in the roof of the mouth that results when the two sides of the palate do not join together during development.


What is Pediatric Cleft Palate?

The palate (mouth) has two main parts – a hard bone portion that is in the front half of the palate and a floppy soft part in the back half of the palate. Run your tongue along the roof of your mouth from your teeth backwards.

  • The front part is hard, because there is bone under this part of the palate.

  • The back part is soft because only small muscles are present within this portion.  

If there is a cleft of the palate, the result is that the two sides of the palate have a gap between them. 

A patient can have cleft palate alone (isolated cleft palate), with a cleft lip or part of a syndrome. Patients with cleft palate alone have different inheritance patterns and characteristics from patients with cleft lip and palate or cleft lip alone.

How common is Pediatric cleft palate?

Cleft palate alone occurs in about 1 in 1,500 children born in the U.S. It occurs more often in girls than in boys. The rates do vary by ethnicity with higher rates (1 in 500) in patients of Asian descent and lower rates (1 in 2,000) in patients of African descent. A cleft lip and palate together is the most common occurrence. It is seen in about 1 in 600 children born in the U.S., occurring more often in boys than girls and more often on the left side than the right side.

There are several factors that may increase the risk of having a child with cleft lip and palate. While the inheritance of many genes from either parent and the maternal use of certain medications and substances (maternal smoking, anticonvulsants, alcohol, retinoic acid) are believed to increase the risk of having a child with a cleft, the majority of children born with a cleft of the lip or palate have none of these associated factors.

The way that the inheritance of many genes can affect the risk for having cleft of the lip or palate is difficult to understand. A simplified way to think about it is that there are many genes that slightly increase someone’s risk of having a cleft. The more of these genes a person has, the more likely it is that they will have a cleft. However, it is important to understand that in most cases, a family with a parent or child with a cleft still has a low risk of having more children with clefts of the lip and palate.

The most common scenario is that a family will have a child born with a cleft and no other history of a person with cleft lip and palate in either parent’s family. The risk of this family’s next child having a cleft is about 5% (1 in 20). If a family has one parent with a cleft but no children with a cleft, the risk of their next child having a cleft is about 5% (1 in 20). If a family has no parent with a cleft but two children born with clefts, the risk of their next child having a cleft is about 10% (1 In 10). If a family has one parent and one child with a cleft, the risk of their next child having a cleft approaches 20% (1 in 5). In other words, a family with one parent and one child born with a cleft has an 80% (4 in 5) chance of their next child NOT being born with a cleft. So even when several family members have had a cleft, the risk is higher than the average person, but still relatively low.

There are rare exceptions to this such as Van der Woude syndrome, which demonstrates autosomal dominant inheritance where 50% of a family’s children may be born with a cleft. For this reason, genetic testing should be done when there is a strong family history of clefts



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