A cleft in the lip
On one side or on both sides; from the small notch in the red border to the gap all the way to the nose.
Discuss your case Cleft upper lip ("hare's lip") is a congenital cleft in the upper lip of a child. It is corrected by surgery in the first months of life, and before that, parents are helped to establish feeding.
CONCEPTUAL VISUALIZATIONA cleft lip is a gap in the upper lip that a baby is born with. It appears when parts of the face do not grow completely during fetal development. The cleft can be on one side or on both sides, from a small notch to a wide gap that reaches the nose, and can be combined with a cleft of the gums and palate.
In everyday life, it is called "hare's lip". This is a colloquial name that can hurt parents and children, so doctors say "cleft lip".
Cleft lip and/or palate is one of the most common birth defects, occurring in about one in 700 babies. According to a large meta-analysis, isolated cleft lip occurs in 0.3 per 1,000 births, and combined cleft palate occurs in 0.45 per 1,000 births.
Most children whose clefts were repaired in time grow up and lead normal lives. The scar after lip plastic surgery fades over the years and becomes less noticeable.
This is general information. What will suit your child, the doctor will tell after the examination.
Cleft lip can be seen immediately after birth, and often on ultrasound during pregnancy.
On one side or on both sides; from the small notch in the red border to the gap all the way to the nose.
When the cleft reaches the nose, the shape of the nostril on the side of the cleft also changes.
The cleft can take over the gums and palate - then the treatment is longer.
Cleft palateIt can be difficult for a child to tightly grasp a breast or a nipple, so it may not be full.
With an isolated cleft lip, accompanying defects occur less often than when combined with a cleft palate, so the child is examined completely.
The exact cause in a particular child is usually not known. The cleft is almost certainly not the result of anything the mother did or didn't do during pregnancy.
The lip is formed in the womb, when parts of the face grow. If they do not converge, a gap remains.
Sometimes genes play a role, but in most cases clefts run in families. If there is already a child with a cleft in the family, the probability for the next child is about 2-8%.
Clefts are linked to smoking and alcohol, obesity, lack of folic acid, and some anticonvulsant medications. In a meta-analysis, women who took folic acid supplements had a lower risk of cleft lip, but the conclusions are cautious.
Sometimes the cleft is part of a wider condition, such as 22q11 deletion syndrome or Pierre Robin sequence.
Sequence by Pierre RobinThe cleft lip itself does not require emergency care - it is treated in a planned manner. But a baby with a cleft, like any baby, can get sick, and some signs require immediate help.
On the same day: the baby is not eating or eating much less than usual, or after surgery the suture is red, swollen, oozing pus, separated, or has a temperature (below the threshold for 103) - call the pediatrician or the surgeon who operated. In the coming days: the child does not gain weight, feeding is difficult. Planned: cleft was seen on ultrasound or after birth - make an appointment to make a plan for feeding and surgery in advance.
Cleft lip is usually seen on a screening ultrasound at 18-21 weeks, but not always: in different studies, conventional ultrasound has detected between 9% and all such clefts. Volumetric 3D ultrasound shows cleft lip more reliably.
If the cleft was not seen on the ultrasound, it is detected immediately after birth or at the first examination of the newborn.
The child is examined completely. If other defects are found, the doctor may recommend a genetic examination.
From the first days, they monitor how the child eats, breathes, sleeps and gains weight.
The surgeon assesses the width of the cleft, the condition of the nose, gums and palate and plans the timing of the operation.
Cleft lip can be repaired with surgery, but treatment begins earlier — with feeding — and lasts for years. Therefore, a team of specialists guides the child.
The main task of the first weeks is for the child to eat and gain weight.
It is not always necessary, but with a wide cleft it can facilitate the operation.
Cheiloplasty is the main operation.
Cleft lip is operated at Dr. Valikhnovskyi's Institute of Surgery in the field of "Congenital Defects Surgery". Cleft treatment is a plan for years: the clinic is responsible for the surgical part, and the orthodontist and speech therapist guide the child together with the surgeon.
Plastic surgeon, candidate of medical sciences, founder of Dr. Valikhnovskyi Institute of Surgery.
Short answers. What is right for you, the doctor will tell you during the consultation.
This is a colloquial name. It can hurt, that's why doctors say "cleft lip".
Almost certainly not. The exact cause is usually unknown; a cleft is very rarely related to something the mother did or did not do during pregnancy.
With an isolated cleft lip, breastfeeding is usually easier than when there is also a cleft palate; a feeding specialist will help. If it doesn't work, special bottles and expressed milk help.
Usually in 3-6 months. Early operations, up to 3 months, are also done; the terms depend on the condition of the child and are discussed with the surgeon.
Yes, a small scar above the lip will remain, but it is placed along the natural lines of the lip, and it fades over the years.
For the most part, a cleft is an isolated case. If there is already a child with a cleft in the family, the probability of the next one is about 2-8%. If one of the parents has a cleft or the child is diagnosed with the syndrome, the risk is assessed by a geneticist.
Some children later need lip or nose correction. Most often, this is the correction of a scar. How many children need it varies greatly between studies, so the plan is made over years.
The figures on the page are from these sources.
Send a photo or ultrasound report and tell us how the baby is eating. The doctor will explain when to operate and what to do before the operation.
Leave your contact details and briefly describe the situation. A coordinator will contact you to agree on the next step.