Gap in the mouth
During the examination, a hole in the palate is visible - a small one at the back or on the entire palate. A gap hidden under the mucous membrane may not be noticed on examination.
Discuss your case Cleft palate ("cleft palate") is a congenital cleft in the palate through which the mouth connects to the nose. It prevents the child from sucking, increases the risk of fluid in the ears and impairs speech without surgery. The cleft is closed surgically, usually at 6–12 months.
CONCEPTUAL VISUALIZATIONThe palate is the "roof" of the mouth that separates the mouth from the nose. During the development of the child in the mother's womb, its halves should grow in the middle. If this did not happen, a gap remains - a cleft palate, a "wolf's mouth" in everyday life.
The cleft is only in the back, soft part of the palate, or it goes through the entire palate to the front. It can be separate or combined with a cleft lip. Sometimes the gap is hidden by the mucous membrane, and it is not noticed immediately.
Cleft palate is one of the frequent congenital defects of the face. Sometimes it is part of a wider condition, such as 22q11 deletion syndrome or Pierre Robin sequence, so the child is also examined by a pediatrician.
Treatment lasts for years: surgery, feeding, hearing, speech, teeth. But most children grow up after treatment and lead normal lives.
This is general information. What will suit your child, the doctor will tell after the examination.
Cleft palate is usually found immediately after birth. The most worries are in the first months, before the operation.
During the examination, a hole in the palate is visible - a small one at the back or on the entire palate. A gap hidden under the mucous membrane may not be noticed on examination.
The child cannot tightly grasp the breast or nipple, swallows a lot of air, milk flows through the nose. In the first months, she may gain weight poorly.
Fluid collects in the middle ear — this is otitis with effusion. Hearing decreases, and often this is only visible on a hearing test.
Without surgery, speech becomes unclear and hoarse: air comes out through the nose during a conversation.
If the gap extends into the gums, nearby teeth may grow crookedly, be missing, or be redundant.
Clear cleftIf the chin is very small, the doctor will check for Pierre Robin consistency. If the child has difficulty breathing, call 103.
Sequence by Pierre RobinThe exact cause for a specific child is mostly impossible to establish. Most likely, the cleft is not related to anything you did or didn't do during your pregnancy.
The tissues that make up the palate have not grown together. The cause of most non-syndromic cases is unknown.
Most cases are isolated. If there is already a child with a cleft in the family or one of the parents had a cleft, the risk for the next child is about 2-8%.
Smoking during pregnancy increased the chances of a cleft by 1.55 times, and passive smoking was even more harmful. Alcohol during pregnancy is also listed as a risk factor by the NHS.
Obesity increased the chances of a cleft by 1.28 times, type 1 diabetes - by 1.75 times.
Lack of folic acid during pregnancy and some anticonvulsant medications early in pregnancy have been linked to fissures.
Sometimes the cleft is part of a wider condition, such as 22q11 deletion syndrome or Pierre Robin sequence.
The cleft itself does not require emergency care: it is treated according to plan. But a baby with a cleft may not eat well, and some signs in any young child require immediate help.
On the same day: the baby refuses to eat, vomits during the day, or you feel that something is wrong with the baby. If your child has recently had surgery, call the surgeon first. In the coming days: feeding lasts a very long time, milk constantly flows through the nose, the child does not gain weight well. Planned: consultation with a surgeon as soon as possible after birth to make a plan, and regular hearing and speech tests.
Cleft lip is often visible on ultrasound, and cleft palate is very difficult to detect on ultrasound.
Usually, a cleft is found immediately after childbirth or during a newborn examination in the first 72 hours.
To check for other defects or syndromes with which the cleft is associated.
From the first weeks of life onwards regularly due to the risk of fluid in the middle ear.
A speech therapist evaluates speech at 18 months, at 3 and 5 years, and more often if necessary.
The main treatment is an operation that closes the cleft and restores the muscles of the palate. Before it, it is important to establish feeding, and after that to monitor hearing, language and teeth while the child grows.
The first weeks and months before the operation.
Operation under general anesthesia.
Hearing is checked regularly; treated by an ENT doctor.
Cleft palate is operated on at Dr. Valikhnovskyi's Institute of Surgery in the field of "Congenital Defects Surgery". Treatment of a cleft is a team for years: in addition to the surgeon, the child is led by an ENT doctor, a speech therapist and an orthodontist.
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.
Sometimes yes, but with a cleft palate, it is less likely: it is difficult for the child to hug the chest tightly. Then the milk is expressed and given from a soft bottle for children with clefts.
Usually at 6-12 months. In a large study, surgery at 6 months was less likely to cause language problems at 5 years than surgery at 12 months. The doctor determines the terms for your child.
The scar after plastic surgery of the palate remains inside the mouth, it is not visible on the face.
In children with cleft palate, fluid often collects in the middle ear and hearing is reduced. Therefore, hearing is checked regularly, and if necessary, shunts or a hearing aid are installed.
Surgery greatly reduces the risk of speech problems, but some children will need a speech therapist, and a small number will need another surgery if their speech remains slurred.
Most likely, no. The exact cause is mostly unknown. The risk is slightly increased by smoking and alcohol during pregnancy, obesity, type 1 diabetes, folic acid deficiency, and some anticonvulsant medications.
Mostly this is an isolated case. If there is already a child with a cleft in the family, the risk for the next one is approximately 2-8%. If the cleft is associated with a syndrome, the risk may be higher.
The figures on the page are from these sources.
Send a photo and statements of the child. The doctor will tell you how to adjust feeding, when to operate and what is needed before the operation.
Leave your contact details and briefly describe the situation. A coordinator will contact you to agree on the next step.