Cleft palate and deafness

Cleft palate or cleft lip and palate can affect many different functions, including speech and hearing. This webpage for parents explains what cleft lip and cleft palate is, the type of deafness commonly associated with cleft palate, and how the deafness can be managed.

What is cleft lip and palate?

Cleft lip is a term used to describe a notch, opening or separation in the upper lip. Cleft palate describes an opening or separation in the roof of the mouth, which is either easily seen, or is covered by the lining of the roof of the mouth (submucous cleft palate).

Boy with a cleft palate

Cleft lip and palate are common and affect about one baby in every 700 births. The degree to which children are affected and the extent of the clefts and their impact on the child varies.

Cleft lip and palate can each occur alone or together. Of the babies born with cleft lip and/or palate, around:

  • 50% have a cleft palate
  • 25% have a cleft lip
  • 25% have both a cleft lip and palate.
A cleft lip, with or without a cleft palate, is more common in boys. Cleft palates on their own are more common in girls. Cleft lip and palate, and cleft palate alone may be more common in babies with close relatives who also have it.

Children who were born with a cleft lip alone are not normally at a greater risk of long-term deafness than the general population. However, children with cleft palate or cleft lip and palate are likely to have longer-term difficulties with their hearing. 

Scott and Siobhan tell us about their son Bayley's cleft palate and glue ear

This video includes information from Dr Raouf Chorbachi, Audiovestibular physician, about cleft palate and hearing loss and the services that are available.

What is the cause of cleft lip and/or palate?

We all start out life with a cleft lip and palate. During early pregnancy these clefts normally fuse together. The exact reasons for isolated cleft lip and/or palate are unclear, although it is usually a random, one-off event. 


My child has a cleft lip and/or palate – what happens now?

Sometimes cleft lip and/or palate are diagnosed during routine antenatal scans. Sometimes they are not known about until birth. When the cleft lip and/or palate are diagnosed you will be referred to a specialist regional cleft lip and palate service. A team of professionals will be involved in the care and treatment of your child. This team may include:

  • a specialist cleft nurse
  • an audiovestibular (hearing and balance) physician
  • an ear, nose and throat (ENT) surgeon
  • a maxillofacial (head, neck, face, jaws) surgeon
  • a plastic surgeon
  • a speech and language therapist
  • an orthodontist
  • an audiologist
  • a psychologist
  • a paediatrician.

The team will also have access to a geneticist and other professionals who may need to be involved in the overall care of your child. The team will discuss with you the appointments, tests, assessments and operations your child will need and together you will develop a care plan.

Hearing tests

As part of your child’s care plan it is important that they have their hearing assessed. This may be done at the regional centre or they may refer you to your local ear, nose and throat (ENT) and audiology service. This will normally be done routinely shortly after birth. Your audiology team will regularly assess your child’s hearing. This should be at least once a year during the first three years, and again around the time your child starts school, and at ages five and 10 years.

For more information on hearing tests see our resource Understanding your Child's Hearing Tests.


Types of deafness and cleft palate

  • Glue ear is the most common type of deafness in children with cleft palate. It's a type of conductive deafness – when sound cannot pass efficiently through the outer and middle ear to the inner ear (cochlea and auditory nerve). Glue ear is a build-up of sticky fluid in the middle ear. It may not cause any problems in hearing or it may cause a mild to moderate deafness (20–60 dB) in the affected ear. For most children without a cleft palate, glue ear is a temporary condition that they grow out of by around eight years old as their Eustachian tube and other cavities grow larger. However, in children with a cleft palate there are likely to be additional structural abnormalities of the Eustachian tube and the muscles may not work as well. Almost all children with a cleft palate will get glue ear before the age of one and it may persist much longer than for other children. For this reason children should be monitored closely.

  • Sensorineural deafness is unusual in children with a cleft palate. This type of deafness may indicate an associated syndrome or, rarely, a co-existing condition (two or more unrelated conditions happening together).

  • Mixed deafness is when children who have conductive deafness, such as glue ear, also have sensorineural deafness.

Your ear, nose and throat (ENT) and audiology services should provide you with information about options including surgery (grommets), medicines and hearing aids.


Grommets and cleft palate

Your surgeon may recommend putting in grommets at the same time as the surgery to replair the cleft palate. In older children grommets may be offered if the glue ear has not cleared up spontaneously following the palate muscle repair.

Children who have a cleft palate are much more likely to have recurring glue ear after the grommets have come out. It is possible to put in grommets up to three times but it is not good practice to carry out repeated grommet surgery after this. This is because every time one is put in the eardrum has to be punctured, and every time one falls out it leaves a tiny scar. 


Cleft palate and hearing technology

Hearing aids

Some ENT doctors and audiologists recommend hearing aids as the preferred management for children with glue ear who also have a cleft palate.

The type of hearing aid that will be suitable for your child will depend on the type and level of deafness they have and whether the outer ear is fully formed.

Girl with hearing aids

Please note the girl pictured above does not have a cleft lip or palate.

A hearing aid sits on the top of the pinna (the outside part of the ear) and is connected to an earmould that is specially made to fit in the child’s ear. Children who have a syndrome associated with a cleft palate may have a very small pinna that can make it difficult to keep a behind-the-ear hearing aid in place. Smaller ear canals can sometimes make it difficult to get well-fitting earmoulds.

Narrow ear canals can cause sound from a behind-the-ear hearing aid to ‘bounce’ back off the wall of the ear canal, causing whistling or ‘feedback’ from the hearing aids. If your child has any of these problems, talk to their audiologist about possible solutions.

Children who have conductive hearing loss and have problems wearing behind-the-ear hearing aids may benefit from a different type of hearing device that allows the child to hear sounds using bone conduction. For more information on bone conduction hearing aids and bone conduction hearing implants (BCHI) visit our bone conduction hearing implants page.

Technology at school

Find out how a radio aid can help children with hearing aids hear better at school, and how a soundfield system can help children with or without hearing aids.


Ear infections and cleft palate

Children with a cleft palate may be more prone to middle ear infections. This is caused by a combination of factors that can encourage bacterial growth in the middle ear. Ear infections can occur with or without glue ear. Any discharge (leak) from the ear is abnormal. If it occurs you should see your GP, who may prescribe oral antibiotics or antibiotic drops. Any prolonged discharge from the ear should be assessed by your ENT doctor.

Swimming and ear infections

Some children appear to get ear infections triggered by swimming. Most doctors feel it is important for children to learn to swim and enjoy swimming rather than worry about possible infection. If your doctor permits swimming, try to stop dirty water entering your child’s mouth or being swallowed. Avoid letting your child swim in lakes or non-chlorinated pools as the water usually has a high bacteria count. 


Syndromes and medical conditions associated with cleft palate

Most children with a cleft palate or cleft lip and palate have no other medical problems associated with it. However, cleft lip and palate occurs in more than 400 syndromes. ‘Syndrome’ means a collection of signs or symptoms that commonly occur together, which doctors recognise as being related. Syndromes may be caused by changes to genes, known as mutations, which are inherited (passed on) from one or both parents to the child. Sometimes the change in the gene happens in the child for the first time. This is known as a new or spontaneous mutation.

For further information about genetic counselling and the genetic causes of deafness, read our booklet Genetic Counselling: Information for families.

About 30% of children born with cleft lip and/or palate have a syndrome. Here is a list of the commonest syndromes.

Van der Woude syndrome

Pierre Robin Sequence
(also known as Pierre Robin syndrome) – Pierre Robin Network

22q11.2 deletion syndrome (sometimes known as DiGeorge syndrome and Velocardiofacial syndrome)

Stickler syndrome – Stickler Syndrome Support Group

Down’s syndrome – read our booklet Down’s Syndrome and Childhood Deafness and visit the Down’s Syndrome Association’s website

CHARGE syndrome – The CHARGE family support group
Hemifacial microsomia
(Goldenhar syndrome) – Goldenhar UK

Treacher Collins syndrome – Treacher Collins Family Support Group

Kabuki syndrome – Kabuki UK


Further information

  • Contact gives support and advice for families with disabled children. 


Acknowledgements and references

We are grateful to Mr Raouf Chorbachi, Consultant Audiovestibular Physician with Great Ormond Street Hospital for Children NHS Trust and North Thames Regional Specialist Cleft Lip and Palate service for his guidance in preparing this webpage.

Full references for this webpage are available by emailing

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Published: October 2015
Review due: October 2017