In this article
Oral clefts appear as splits or openings in the upper lip, palate (roof of the mouth), or both. The splits cause gaps and defects in the affected areas. They are also usually associated with a nose deformity on the same side.
Orofacial clefts, specifically a cleft lip or palate, are among the most common head and neck birth defects. Clefts affect roughly 1 in 700 children worldwide.
In the U.S., cleft lip/palates are most common in Native Americans, Asians, and Latinos. African Americans have the lowest risk of developing orofacial clefts.
Cleft palate children may have speech and language problems. However, it can also lead to serious medical and dental issues.
These conditions include:
Half of all clefts involve both the lip and palate. A cleft that only affects the palate is a less common birth defect.
Common medical conditions associated with cleft lip and palate include:
Cleft lips can either be complete or incomplete, which means the splits may or may not extend to the nose. They can also develop on one side (unilateral) or both sides (bilateral) of the upper lip.
There are a few types of cleft lips:
Clefts that develop on one side of the upper lip and do not extend into the nose.
Clefts that develop on one side of the upper lip and extend into the nose.
Clefts that appear on both sides of the upper lip but do not extend into the nose.
Clefts that appear on both sides of the upper lip and extend into the nose.
Like cleft lips, cleft palates can be complete or incomplete, meaning the splits may involve the primary (front) palate, secondary (back) palate, or both.
There are a few types of cleft palates:
Clefts that develop in the soft palate (back of the mouth).
Clefts that develop in the soft and hard palate on one side of the mouth. The splits extend past the lips and into the nose.
Clefts that develop in the soft and hard palate on one side of the mouth. The splits extend past the lips and into the nose.
Clefts that develop in the soft and hard palate on both sides of the mouth. The splits extend past the lips and into the nose.
A submucous cleft palate affects the palate and uvula, the teardrop-shaped tissue hanging in the back of your throat. The soft palate and uvula work together to prevent food from going up your nose.
Someone with a submucous cleft palate has a cleft underneath the mucous membrane. This type of cleft is “hidden” and will not be noticeable until the baby is born. It develops in about 1 in 1,200 babies.
A term used when a cleft occurs in the palate only, with no cleft lip present. One in 2,000 babies are born with this type of cleft. It’s also typically difficult to see.
Clefts are birth defects caused by genetic and environmental factors. Common reasons a child may develop a cleft lip and/or palate include:
Some medications can affect your baby during pregnancy and increase the likelihood of a cleft lip or palate.
These medications include, but are not limited to:
A prenatal ultrasound can detect a cleft lip or palate after 16 weeks of pregnancy. The diagnosis is confirmed at birth with a physical examination.
An incomplete cleft lip or an isolated palate may not be seen on an ultrasound. Because of this, these types of clefts can be diagnosed for the first time at birth.
They’ll also perform a comprehensive exam to determine if the cleft involves both the soft and hard palate or the soft palate alone. In some cases, a cleft is diagnosed on a fetal MRI.
Children born with a cleft lip, palate, or both require multiple phases of treatment starting from birth and into early adulthood (18+ years old). Treatment typically includes:
Cleft lip and palate repairs are performed by a plastic surgeon, pediatric otolaryngologist, or an oral and maxillofacial surgeon with extensive training in pediatric craniomaxillofacial surgery. There are a few phases of treatment throughout childhood, depending on the child’s needs.
Children with cleft lip and palate from birth require pre-surgical infant orthopedics (PSIO). In particular, this procedure reshapes nasal and alveolar segments before cleft lip surgery.
Most babies typically have surgery early in life to repair cleft lip and palate, typically between 3 and 6 months of age. A nasolabial (lip) adhesion may also be necessary before repairing the cleft lip to reduce tension and speed up recovery.
A cleft palate repair is completed between 9 and 18 months, typically around age 1. Early palate repair allows for better speech development.
Repairing the defect early creates more scar tissue and may lead to improper mouth growth, improper bite, and poor facial esthetics. Orthodontic treatment is typically necessary later on to correct these issues. If palate repair is completed after 18 months, speech can be negatively impacted.
Velopharyngeal insufficiency (VPI) occurs when the soft palate does not close tightly against the back of the mouth. This typically leads to abnormal speech and/or hypernasality. Velopharyngeal surgery is completed around 3 years of age if a child’s speech does not improve.
After a cleft lip and palate repair, a surgeon performs alveolar bone graft surgery a few years later. The surgery adds bone to the gum ridge in children born with clefts. In addition, the bone graft must be completed as a child begins to lose their baby teeth before permanent teeth grow.
As baby teeth fall out and permanent teeth grow in (the mixed dentition phase), the first round of orthodontic treatment occurs. Orthodontic treatment typically:
By age 13, all permanent teeth have erupted. An additional phase of orthodontic treatment may also be necessary to align teeth and fix any dental abnormalities.
Orthognathic surgery is an operation that corrects the alignment of the jaws. It may be necessary after the cleft lip repair, bone graft surgery, and orthodontic treatment.
Ways to help prevent cleft lip during pregnancy include:
In this article
6 min read
4 min read
Less than a minute.
4 min read
5 min read
4 min read
