Cleft Lip and Palate


Story Comments Share
Updated: 1/06/2009 6:11 pm | Published: 1/06/2009 10:39 am
Craniofacial Foundation of Utah
A Non-Profit Organization
(801) 743-0700
www.cranioutah.com

The Craniofacial Foundation of Utah, a non-profit organization, was founded by Dr. Louis Morales, Jr., one of the nation’s leading authorities in Plastic and Craniofacial Surgery.

Cleft palate is a treatable birth defect in which the baby's roof of the mouth (palate) does not develop normally during pregnancy, leaving an opening (cleft) that may go through to the nasal cavity. Cleft palate may involve any part of the palate, including the front part of the roof of the mouth (hard palate) or the small tag of tissue that hangs down from the soft palate (uvula). It may also occur by itself or along with other birth defects of the face and skull, particularly cleft lip.

Cleft palate and cleft lip are the most common congenital defects of the head and neck.1 Until treated surgically, cleft palate can interfere with feeding, speech development, and hearing.

See pictures of two different types of cleft palate and two types of cleft lip.

What causes cleft palate?
Cleft palate may be caused by genetic and environmental factors, although the exact relationships are not clearly understood. If you were born with a cleft palate, your children will have an increased risk for the defect.

A baby may be at higher risk for being born with cleft palate if during pregnancy the mother uses certain medicines, is exposed to radiation or infections, takes illegal drugs, smokes, or drinks alcohol.

What are the symptoms?
Some forms of cleft palate are obvious at birth because they produce distinctive facial deformities. But the way a newborn's face looks does not always indicate the seriousness of the condition. The most reliable indicator of severity is the location of the cleft. For example, a nonvisible small cleft in the soft palate may have greater long-term impact-because of its effect on speech-than a visible large cleft.

Babies with cleft palate generally have feeding problems because they are not able to suck and swallow normally.

How is cleft palate diagnosed?
Cleft palate is diagnosed by a physical exam shortly after birth.

Fetal ultrasound can sometimes detect cleft palate as early as 14 to 16 weeks of gestation, especially if it is severe and occurs along with a cleft lip. But fetal ultrasound is not reliable for this purpose.

How is it treated?
Treatment for cleft palate usually involves a team of doctors and other health professionals. A doctor or nurse can guide you on how to feed and care for your baby.

Surgery is done to correct the defect, usually when your child is between 12 months and 18 months of age. More than one procedure is often needed. Surgical corrections specifically for cleft palate usually are completed by your child's teen years.

Some children with cleft palate develop problems that require special treatment, such as speech and hearing difficulties, sinus and ear infections, or complications following surgery to correct cleft palate. Dental problems sometimes also occur, such as having extra, misshapen, or missing teeth.

Source: WebMD.com

Story Comments Share
2 Comment(s)
Comments: Show | Hide

Here are the most recent story comments.View All

The views expressed here do not necessarily represent those of ABC4

kati - 1/6/2009 8:57 PM
Thank you, thank you, thank you for this segment. I myself and my son have bilateral cleft lip and palate. It is the number one birth defect in Utah and a lot of people don't know anything about it. The whole cranio facial team at Primary Childrens Hospital are miracle workers. It is so emotional to have a child with a genetic birth defect, i know i felt like the worst mother in the world for doing this to my son. Everyone focuses on the post-operative results, but it is so hard to see your beautifel baby that you have fallen in love with, that beautiful face and mouth, change. Your baby leaves your arms perfect in your eyes, and they return to you different. It is an emotion that i hope i don't have to feel again. I love my little guy and he is so brave and so strong. AT 18 months, he is my little hero!!! I also have a new love for my own mom and what she went through when i was born 27 years ago, when this was even more uncommon. Thank you Alicia for sharing your beautiful sons and your story. I couldn't help but cry. --Thanks Kati and Carter

missymoo - 1/6/2009 6:36 PM
I think it was great that you guys talked about Cleft Lip and Palate on your show today! I have a 10 year old niece that was born with Cleft Lip and Palate, Dr. Morales is also one of her doctors, I've heard great things about him. My niece also went through speech therapy and she talks perfectly now, & she is one of the most beautifull, sweet girls ever!! Thank you for bringing this to peoples attention!!


Inergize Digital This site is hosted and managed by Inergize Digital.
Mobile advertising for this site is available on Local Ad Buy.