ConditionChildren's health

Cleft Lip and Palate

Cleft lip and palate are birth differences in which the upper lip, the roof of the mouth (palate), or both do not fully join during early pregnancy, leaving a gap. Together they are among the most common birth differences, affecting roughly 1 in 700 babies worldwide. A specialist cleft team repairs the lip at about 3 months and the palate by 6 to 12 months, then supports feeding, hearing, speech and teeth through childhood. Most children grow up healthy.

Also called: Orofacial cleft, cleft lip, cleft palate, cleft lip with or without cleft palate (CL/P)

At a glance

What it is
A gap in the upper lip, the roof of the mouth, or both, present from birth.
How common
About 1 in 700 births worldwide. Cleft lip with palate is more common in boys, cleft palate alone in girls.
Causes
A mix of genes and environment. Smoking, some medicines and low folic acid in pregnancy raise risk.
Diagnosis
Cleft lip is often seen on the 18 to 21 week ultrasound. Cleft palate alone is usually found at birth.
Treatment
Lip repair at about 3 months, palate repair at 6 to 12 months, then team care for feeding, ears, speech and teeth.

When to get help

Call 911 or go to the ER

  • A baby with a cleft who has pauses in breathing, turns blue, or struggles to breathe when lying on their back
  • Choking or color change during every feed

See a doctor within a day or two

  • Poor feeding with fewer than 6 wet diapers a day, or weight loss after the first week
  • Fever of 38 °C (100.4 °F) or more in a baby under 3 months
  • Bleeding, wound opening, fever or refusing fluids after cleft surgery

Book a routine appointment

  • Repeated ear infections or signs your child is not hearing well
  • Nasal-sounding speech, or speech that is hard to understand by age 3
  • Questions about the chance of a cleft in a future pregnancy

What cleft lip and palate are

The lip and palate form from separate pieces of tissue that grow toward each other and fuse. The lip joins between about weeks 4 and 7 of pregnancy and the palate between weeks 6 and 12. When fusion is incomplete, a cleft remains.

TypeWhat it looks likeMain issues
Cleft lip onlyA notch or full split in the upper lip, sometimes reaching the noseAppearance; feeding usually manageable
Cleft lip and palateSplit lip plus an opening in the roof of the mouthFeeding, ears, speech, teeth and gums
Cleft palate onlyOpening in the roof of the mouth, lip normalFeeding, ears, speech; more often linked to a syndrome
Submucous cleftThe palate muscle is split under intact liningOften missed until speech problems appear

A cleft lip can be unilateral (one side, more often the left) or bilateral (both sides). It can be incomplete, a small notch, or complete, running into the nostril. For more on clefts that affect only the roof of the mouth, see our page on cleft palate.

Causes and risk factors

Most clefts have no single cause. They come from a combination of genes and factors in early pregnancy.

  • Family history: the chance rises if a parent or sibling has a cleft.
  • Syndromes: about 1 in 3 children with cleft palate alone, and fewer with cleft lip, have an associated genetic syndrome, such as 22q11.2 deletion syndrome, Van der Woude syndrome or Pierre Robin sequence.
  • Smoking in pregnancy clearly increases risk.
  • Alcohol in pregnancy, including as part of fetal alcohol syndrome.
  • Certain medicines taken in early pregnancy, including some anti-seizure drugs (such as topiramate and valproate).
  • Diabetes before pregnancy and obesity.
  • Low folic acid intake around conception.

Nothing a parent did in most cases caused the cleft. Many occur with no identifiable risk factor.

Diagnosis

Cleft lip is often seen on the routine anatomy ultrasound at 18 to 21 weeks. Cleft palate alone is hard to see on ultrasound and is usually found during the newborn exam, when a doctor looks at and feels the roof of the mouth. A submucous cleft may only be suspected later, from a split uvula, a notch in the hard palate, or nasal speech.

After a prenatal diagnosis, parents are usually referred to a cleft team before birth. A genetic assessment may be offered, especially for cleft palate alone or when other differences are found.

Feeding a baby with a cleft

Feeding is the first practical challenge, because a cleft palate stops a baby from making suction.

  • Cleft lip only: many babies breastfeed well. The breast can fill the gap.
  • Cleft palate: breastfeeding directly is usually not effective. Expressed breast milk or formula is given with special squeezable bottles or valve bottles that let a caregiver help milk flow.
  • Feed in a fairly upright position to reduce milk coming out of the nose.
  • Burp often, because babies with clefts swallow more air.
  • Feeds should take no more than about 30 minutes. Longer feeds burn too many calories.
  • A cleft nurse will check weight closely in the first weeks.

Cleft lip and palate surgery timeline

Timing varies between teams, but a typical plan is:

AgeTreatment
Before surgerySome teams use nasoalveolar molding (a plate and tape) to narrow a wide cleft
About 3 monthsCleft lip repair, often with initial nose reshaping
6 to 12 monthsCleft palate repair, before speech develops
3 to 5 yearsSurgery for speech if the palate does not close off the nose well (velopharyngeal insufficiency)
8 to 11 yearsBone graft to the gum line before the adult canine tooth comes in
TeensOrthodontics, sometimes jaw surgery, and nose or lip revision when growth is complete

Repairs are done under general anesthesia. Babies usually stay in hospital for 1 to 3 days.

Long-term care and complications

A team that includes a surgeon, specialist nurse, speech therapist, audiologist, orthodontist, dentist and psychologist follows children until adulthood.

  • Ears and hearing: the muscles that open the ear tube attach to the palate, so fluid behind the eardrum (otitis media with effusion) is very common. Hearing is tested regularly and ear tubes are often needed.
  • Speech: some children have nasal-sounding speech or difficulty with certain sounds even after repair. Speech therapy helps most.
  • Teeth: missing, extra or misplaced teeth near the cleft are common, and orthodontic treatment is usually needed.
  • Emotional wellbeing: most children adjust well. Teams screen for teasing, self-esteem issues and anxiety.

Outlook and prevention

With modern team care, children born with cleft lip and palate usually eat normally, speak clearly and have good facial appearance. They go to mainstream school and lead ordinary lives. Outcomes are less certain when a cleft is part of a wider syndrome.

To lower risk in a future pregnancy, take folic acid (at least 400 micrograms daily) from before conception, avoid smoking and alcohol, manage diabetes, and review any regular medicines with a doctor before trying to conceive.

Frequently asked questions

What causes cleft lip and palate?

It is caused by a mix of inherited genes and factors during early pregnancy, when the lip and palate are forming. Smoking, alcohol, some anti-seizure medicines, diabetes and low folic acid increase the risk. In many babies there is no clear cause, and nothing the parents did caused it.

Can cleft lip be seen on an ultrasound?

Often, yes. Cleft lip is usually visible on the anatomy scan between 18 and 21 weeks, especially when it is complete. A cleft palate without a cleft lip is much harder to see on ultrasound and is usually found when the baby is examined after birth.

At what age is cleft lip surgery done?

Most teams repair a cleft lip at around 3 months of age, when the baby is gaining weight well and anesthesia is safe. The palate is repaired later, usually between 6 and 12 months, so it is closed before the child starts to talk.

Can a baby with a cleft lip breastfeed?

Many babies with a cleft lip only can breastfeed, because breast tissue fills the gap and allows a seal. Babies with a cleft palate usually cannot create suction, so they are fed expressed breast milk or formula using special bottles. A cleft nurse can help you choose a method.

Is cleft lip and palate genetic?

Partly. A family history increases the chance, and some clefts are part of genetic syndromes. If one parent or child is affected, the chance in a future child is a few percent rather than the general 1 in 700. A genetic counselor can give a more precise figure for your family.

Sources

This guide was written from current patient and clinical guidance, including:

  • CDC: Facts about cleft lip and cleft palate
  • American Cleft Palate-Craniofacial Association: Parameters for evaluation and treatment of patients with cleft lip/palate
  • NHS: Cleft lip and palate
  • MedlinePlus: Cleft lip and palate
  • World Health Organization: Congenital disorders