A baby with a cleft might have:
- only a cleft palate
- only a cleft lip
- both a cleft lip and a cleft palate
What Causes Cleft Palate?
During the first 6 to 10 weeks of pregnancy, the bones and skin of a baby’s upper jaw, nose, and mouth normally come together (fuse) to form the roof of the mouth and the upper lip. A cleft palate happens when parts of the roof of the mouth do not fuse together completely.
Doctors don’t always know why a baby develops a cleft, though some clefts may be related to genetic (inherited) factors. Also, some environmental factors can increase the risk of a birth defect, such as:
- taking certain medicines (such as some anti-seizure medicines) during pregnancy
- not getting the right amount of prenatal nutrients
- exposure to some chemicals during pregnancy
- smoking cigarettes, using drugs, and/or drinking alcohol during pregnancy
How Is a Cleft Palate Diagnosed?
Newborns have an oral exam soon after they’re born. Doctors usually find a cleft palate when they examine the inside of a baby’s mouth during this exam.
How Is a Cleft Palate Treated?
A cleft palate usually is repaired with surgery called palatoplasty (PAL-eh-tuh-plass-tee) when the baby is 10–12 months old. The goals of palatoplasty are to:
- Close the opening between the nose and mouth.
- Help create a palate that works well for speech.
- Prevent food and liquid from leaking out of the nose.
In this surgery, a plastic surgeon will:
- Close the cleft in layers.
- Rearrange and repair the muscles of the soft palate so they work better during speech.
- Make two incisions (cuts) on each side of the palate behind the gums to ease tension on the palate repair.
This surgery requires general anesthesia and takes about 2–3 hours. Most babies can go home after 1 or 2 days in the hospital. The stitches will dissolve on their own.
Your child will need a liquid diet for a week or two, then will eat soft foods for several more weeks before going back to a regular diet. You may be asked to keep your baby in special sleeves (“no-nos”) that prevent the elbows from bending. This is so your baby can’t put any fingers or hard objects into the mouth, which could make the cleft palate repair come open.
When Should I Call the Doctor?
Cleft palate surgery has greatly improved in recent years. Most kids who undergo it have very good results. There are risks with any surgery, though, so call the doctor if your child:
- has a fever above 101.4°F (38.5°C)
- has lasting pain or discomfort
- has heavy bleeding from the mouth or nose
- won’t drink fluids
- isn’t making wet diapers
What Else Should I Know?
A child with a cleft palate can sometimes have other health problems, such as:
- trouble breathing
- frequent ear infections
- trouble feeding
- hearing loss
- eye problems
- speech difficulties
It’s important to work with a care team experienced in treating children with cleft lip and palate. Besides the pediatrician, a child’s treatment team will include:
- plastic surgeon
- ear, nose, and throat (ENT) physician (otolaryngologist)
- speech-language pathologist
You might also work with:
- an oral surgeon
- a social worker
- a psychologist or therapist
- a geneticist
- a team coordinator
Some kids with cleft palate may need other surgeries as they get older. These might include:
- Speech surgery: Children can develop speech problems even after the palate has been repaired. At your regular appointments with the cleft team, the speech-language pathologist will carefully listen to your child’s speech to help the surgeon decide if another surgery is needed to improve speech.
- Orthognathic (or-thig-NATH-ik) surgery: Some children with cleft palate need this surgery to realign the jaws and teeth when they’re older. It’s done when the child is finished growing.
Most kids with cleft palate are treated successfully with no lasting problems. A team experienced in treating children with cleft lip and palate can create a treatment plan tailored to your child’s needs.
The psychologists and social workers on the treatment team are there for you and your child. So turn to them to help guide you through any hard times. You also can find more information and support online:
- American Cleft Palate-Craniofacial Association (ACPA)
- Cleft Lip & Palate Association
- FACES: The National Craniofacial Association
- Smile Train
Content retrieved from: https://kidshealth.org/en/parents/cleft-palate.html.