Cleft upper lip means there is a gap or split in the baby’s upper lip that did not join together properly before birth. The split can look like a small notch or a wide opening, and it may go up toward the nose. It happens very early in pregnancy when the tissues of the face are forming and do not fuse completely.
A cleft upper lip (also called cleft lip) means the upper lip did not join fully while a baby was growing in the womb. It can look like a small notch or a wider gap that may reach the nose. It can happen on one side or both sides. Cleft lip can occur alone or with cleft palate (an opening in the roof of the mouth). The good news is that cleft lip is treatable, and most children do very well with the right care team and surgery plan. 1
Cleft upper lip is a type of orofacial cleft. It can happen alone or together with a cleft in the roof of the mouth, called a cleft palate. Babies with cleft upper lip may also have problems with feeding, ear infections, teeth, and speech if it is not treated by a special cleft team.
Doctors know that cleft upper lip is common all over the world. It appears in about 1 in 700 births when you include cleft lip with or without cleft palate. Most children can do very well after surgery and proper care from a team that includes surgeons, speech therapists, and dentists.
Other names
Cleft upper lip is usually called cleft lip in medical books and guidelines. The word “cleft” means a split or opening, and it describes the gap seen in the upper lip.
Sometimes older books use the word “harelip” because the lip can look like the lip of a hare or rabbit. Today, doctors avoid this word because many people find it hurtful and disrespectful. They prefer the kind and correct term “cleft lip” or “cleft upper lip.”
You may also see names like “unilateral cleft lip” when the split is on one side, or “bilateral cleft lip” when it is on both sides. When the cleft lip is present with a cleft palate, many sources write it as “cleft lip and palate.”
Types
Doctors describe types of cleft upper lip based on which side is affected and how large the gap is. This helps them plan the best surgery and follow-up care.
Unilateral incomplete cleft upper lip – The split is on one side of the lip and does not reach all the way up into the nose. It may look like a notch or groove.
Unilateral complete cleft upper lip – The split is on one side and goes all the way from the lip into the nostril. The nose on that side may look pulled or flattened.
Bilateral complete cleft upper lip – There are two splits, one on each side of the upper lip, and both go into the nose. The middle part of the lip may look like it is hanging or pushed forward.
Bilateral incomplete cleft upper lip – Both sides of the lip have a gap, but the splits do not fully reach the nose. The changes can be milder than in the complete form.
Midline cleft upper lip – The split is in the center of the upper lip. This type is rare and is more often linked with other brain or facial problems.
Microform cleft upper lip – This is a very mild type. It may look like a small dent, thin white line, or scar on the upper lip, but the underlying lip muscle can still be affected.
Causes
Doctors believe cleft upper lip has many causes working together, including genes and things in the environment. Often, no single cause is found for one baby, but research has shown several strong risk factors.
1. Genetic factors (family history)
If a parent, brother, sister, or close relative has a cleft lip or cleft palate, the risk is higher for the baby. This is because some genes that control facial growth can be passed down in families. Still, even with a family history, parents often do nothing wrong; it is just how the genes combine.
2. Specific genetic syndromes
Cleft upper lip can be part of a larger genetic syndrome, such as certain craniofacial or developmental syndromes. In these cases, the child may also have other features, like limb, heart, or brain differences. Genetic testing can help find the exact syndrome.
3. Chromosomal problems
Changes in the number or structure of chromosomes, such as deletions or duplications, can affect how the face forms in early pregnancy. These chromosomal changes may lead to cleft lip along with other birth differences.
4. Maternal smoking during pregnancy
Studies show that women who smoke during pregnancy have a higher chance of having a baby with cleft lip or palate. The chemicals in cigarette smoke may disturb blood flow and the delicate steps of facial fusion in the first weeks of pregnancy.
5. Maternal alcohol use
Heavy drinking in early pregnancy can harm the embryo’s facial development. Alcohol can interfere with cell growth and migration, which are needed for the lip parts to join, leading to clefts and sometimes other facial anomalies.
6. Certain medicines in early pregnancy
Some medicines taken in the first trimester (for example, some anti-seizure drugs, acne drugs with retinoic acid, or certain blood thinners) have been linked to a higher risk of cleft lip. Doctors try to use safer alternatives for women who are pregnant or planning pregnancy whenever possible.
7. Poor folic acid intake
Folic acid is a B-vitamin that helps cells divide and tissues close correctly. Low folic acid levels around conception are strongly linked to spinal defects and may also play a role in cleft lip risk. Prenatal vitamins with folic acid are usually recommended.
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9. Maternal obesity
Being very overweight before pregnancy is another known risk factor. Excess body fat can change hormones and inflammatory signals, which may influence how the face and lip tissues form.
10. Maternal infections and high fever
Certain infections or high fever early in pregnancy may interfere with normal facial development. When the mother’s body is stressed by severe illness, the embryo can be more vulnerable to developmental errors.
11. Exposure to harmful chemicals
Contact with some industrial chemicals, pesticides, or heavy metals during early pregnancy has been studied as a possible risk. These substances may damage DNA or affect the way genes are turned on and off during facial development.
12. Radiation exposure
High doses of ionizing radiation in early pregnancy (for example, from major radiation accidents or repeated high-dose scans) can disturb organ formation. This can sometimes include orofacial clefts, although it is rare in usual medical care.
13. Very early pregnancy without prenatal care
Women who do not receive prenatal care may miss advice about vitamins, medicine safety, and lifestyle. Lack of this support can increase the chance that preventable risk factors, like smoking or poor nutrition, remain uncorrected in the first weeks.
14. Advanced maternal age
Babies born to older mothers have a slightly higher risk of some birth defects. Age can increase the chance of genetic or chromosomal errors, which may include those linked with cleft lip.
15. Consanguinity (parents closely related)
When parents are closely related (for example, cousins), they may share the same rare genes. If both pass such a gene to the baby, it can result in certain birth defects, including cleft lip, in some families.
16. Poor overall maternal nutrition
Not eating enough healthy food, proteins, vitamins, and minerals before and during early pregnancy may increase the risk of several congenital defects. The growing lip needs a steady supply of nutrients to form and fuse properly.
17. Maternal use of illegal drugs
Some illegal drugs can harm the developing embryo by reducing oxygen, changing blood flow, or directly damaging cells. This may raise the risk of orofacial clefts in addition to many other health problems.
18. Environmental tobacco smoke (second-hand smoke)
Even if the mother does not smoke, breathing in smoke from others can expose her and the baby to many of the same toxic chemicals. This can increase the risk of cleft lip slightly, as suggested by population studies.
19. Male sex of the baby (risk factor)
Cleft lip with or without cleft palate is more common in male babies than in females. Sex is not a “cause,” but it is a risk factor that shows there are biological differences in how boys and girls form their faces before birth.
20. Unknown or multifactorial causes
In many babies, no clear single cause can be found. Experts believe that most cases happen because several small genetic and environmental factors come together at a sensitive time in early pregnancy. This is called a multifactorial cause.
Symptoms
Cleft upper lip is usually seen right after birth, but some related problems appear later as the child grows. Not every child will have all the symptoms listed here, but these are common issues doctors and parents watch for.
1. Visible split in the upper lip
The main symptom is a visible gap, notch, or opening in the upper lip. It may be small or large and may be on one side, both sides, or in the middle. This is usually clear as soon as the baby is born.
2. Opening that extends into the nose
In complete cleft upper lip, the split reaches up into the nostril. The nose may look wider on one side, and the base of the nose can appear pulled or twisted.
3. Trouble latching onto breast or bottle
Because the lip cannot form a tight seal around the nipple, babies may have difficulty sucking. They may slip off the nipple or seem to tire quickly while feeding.
4. Milk leaking from the nose or mouth
When a cleft lip is present with a cleft palate, milk can escape into the nose during feeds. Even with only cleft lip, the flow of milk can be less well controlled, leading to dribbling and leaking.
5. Slow weight gain or poor growth
Feeding difficulties can mean the baby does not take in enough milk. Over time, this can cause slow weight gain or “failure to thrive” if feeding support is not given early.
6. Choking, coughing, or gagging while feeding
Some babies with cleft upper lip cough or choke more often when they drink, because they cannot control the flow of milk well. Special bottles and feeding positions can reduce this problem.
7. Frequent ear infections
If a cleft palate is also present, the tube that drains fluid from the middle ear may not work well. Fluid can build up and cause repeated ear infections, which may need ear tubes.
8. Hearing problems
Long-term fluid and infections in the middle ear can affect hearing. Mild to moderate hearing loss is common if ear problems are not treated early.
9. Nasal-sounding voice
Children with cleft lip and palate may have too much air escaping through the nose during speech. Their voice may sound very nasal, and some sounds are hard to make clearly.
10. Difficulty making certain speech sounds
Sounds that require good lip closure, such as “p,” “b,” and “m,” can be hard for children with a cleft upper lip, especially before repair. They may substitute other sounds, which can make speech hard to understand.
11. Dental problems near the cleft
Teeth near the cleft may be missing, extra, small, or twisted. The upper jaw may be narrow or misaligned, and the bite may not fit properly. Orthodontic treatment is often needed.
12. Changes in nose shape
The nostril on the cleft side may look collapsed, wide, or pulled up. The middle part of the nose may be off-center. These changes can affect both appearance and airflow.
13. Sinus and nasal problems
Because the normal structure of the nose and upper jaw is disturbed, some children have blocked noses or sinus infections more often. This can cause mouth breathing and snoring.
14. Social and emotional impact
Visible differences in the face can affect how a child feels about themselves and how others treat them. Some children may experience teasing or low self-esteem and may need emotional support or counseling.
15. Anxiety in parents and caregivers
The birth of a baby with cleft upper lip can cause strong emotions and worry in the family. They may feel guilty or fear the future. Support from the cleft team and parent groups is very important.
Diagnostic tests
Babies with cleft upper lip need careful evaluation by a full cleft and craniofacial team. This team often follows guidelines such as the Parameters of Care from the American Cleft Palate-Craniofacial Association (ACPA) and other national clinical practice guidelines.
Physical exam tests
1. Newborn general physical examination
Soon after birth, the doctor checks the baby from head to toe. They look at the face, mouth, heart, limbs, and organs to see if the cleft is isolated or part of a wider syndrome. This exam guides which extra tests are needed.
2. Detailed facial and lip examination
The doctor carefully inspects the upper lip, nose, and nearby skin to see the exact side, size, and type of cleft. They check whether it is complete or incomplete and whether one or both sides are involved. This helps plan the best surgical repair.
3. Oral cavity and palate examination
Using a light and sometimes a small tongue depressor, the doctor looks inside the mouth for a cleft palate, a split uvula, or other structural problems. Identifying a hidden or submucous cleft palate is important, because it strongly affects speech and feeding.
4. Growth and nutrition assessment
The baby’s weight, length, and head size are measured and compared against growth charts. Poor growth may show that feeding is not going well and that the child needs special feeding support or a nutrition plan.
Manual tests
5. Feeding observation and assessment
A nurse or feeding specialist watches the baby during breast or bottle feeding. They look at how the baby latches, how long they can feed, and whether they cough or choke. This helps decide if special bottles, nipples, or feeding positions are needed.
6. Suck–swallow–breathe coordination test
With a gloved finger or nipple in the baby’s mouth, the clinician gently feels how well the baby sucks and coordinates swallowing with breathing. Poor coordination can increase the risk of choking and may need tailored feeding strategies.
7. Speech and language evaluation
When the child is older, a speech-language pathologist listens to how the child produces sounds and words. They check for nasal speech, unclear sounds, or compensatory habits. This evaluation guides speech therapy and decisions about further surgery if needed.
8. Dental and bite (occlusion) examination
A pediatric dentist or orthodontist looks at the teeth and jaw relationship. They check for missing teeth, crowding, or incorrect bite. This manual exam helps decide when braces, plates, or other dental treatments are needed.
Laboratory and pathological tests
9. Routine pre-surgery blood tests (CBC, electrolytes)
Before cleft lip repair surgery, basic blood tests are done to check hemoglobin, white cells, platelets, and body salts. These tests help make sure the baby is healthy enough for anesthesia and surgery.
10. Coagulation profile (clotting tests)
Blood clotting tests such as PT and aPTT are often measured before surgery. Abnormal results may show a bleeding problem that must be corrected or watched closely during and after the operation.
11. Chromosomal karyotype or microarray
If the child has other birth differences or developmental delays, doctors may order chromosomal testing. This looks for extra or missing pieces of chromosomes that could explain a syndrome that includes cleft upper lip.
12. Targeted gene panel for cleft-related syndromes
Special gene tests can look for known genes linked with cleft lip and palate and certain craniofacial syndromes. Finding a clear gene cause can help with prognosis and family planning for future pregnancies.
Electrodiagnostic tests
13. Newborn hearing screening (OAE or ABR)
Most hospitals screen the baby’s hearing soon after birth. Tests like otoacoustic emissions (OAE) and auditory brainstem response (ABR) record tiny signals from the ear or hearing nerve. These tests are very important because ear fluid and infections are common in cleft conditions.
14. Detailed auditory brainstem response (ABR) test
If the screening shows a problem or if the child gets many ear infections, a more detailed ABR test may be done. It measures how sound signals travel along the hearing nerve to the brainstem and helps decide if hearing aids or ear tubes are needed.
15. Electrocardiogram (ECG) before anesthesia
Some centers record an ECG to check the heart rhythm before surgery, especially if the child has other medical issues. A normal ECG helps the anesthesiologist plan safe anesthesia and monitor the heart during the operation.
Imaging tests
16. Prenatal ultrasound
Cleft upper lip can often be seen on routine pregnancy ultrasound around 16–20 weeks, and in some centers even earlier. Seeing the cleft before birth gives parents time to meet the cleft team and plan delivery and early care.
17. Detailed fetal anomaly scan or 3D ultrasound
Special high-resolution or 3D ultrasound can show the face in more detail. It helps confirm the cleft, look for a cleft palate, and search for other structural differences in the heart, brain, or limbs.
18. Postnatal craniofacial CT scan
Later in childhood, a CT scan of the face and skull may be used to plan complex surgeries. It gives a three-dimensional picture of the bones, nasal passages, and upper jaw, which helps surgeons correct the shape and improve function.
19. Dental panoramic X-ray
A panoramic dental X-ray shows all the teeth and jaws in one picture. It helps the dentist see missing, extra, or poorly positioned teeth and plan timing of orthodontic treatment or bone grafts to the gum ridge.
20. Nasopharyngoscopy or videofluoroscopy for speech
In older children with speech problems, specialists may use a small camera through the nose (nasopharyngoscopy) or moving X-ray (videofluoroscopy) to watch how the soft palate and throat move during speech. This imaging helps decide if more surgery or a speech device is needed.

