Treacher Collins Syndrome
Children born with Treacher Collins syndrome have one or more facial differences. At Children’s Health, our craniofacial surgeons are experts at evaluating and treating syndromes of the head and face. From mild facial differences to severe changes affecting breathing, our highly skilled team can create a custom treatment plan that’s right for your child and family.
What is Treacher Collins Syndrome?
Treacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. The most common symptom is underdeveloped facial bones, which may vary from very mild to severe. A cleft, or hole, may also be present in the palate. The syndrome may also affect a child’s eyes, their ability to breathe, external ear formation or their hearing. Typically, Treacher Collins syndrome doesn’t impact learning nor limit intellectual development.
What are the signs and symptoms of Treacher Collins Syndrome?
Symptoms of Treacher-Collins syndrome include:
Ear
Missing or misshapen external ear structure (anotia, microtia)
Missing or misshapen internal ear structure (less common)
Small or missing ear canals (atresia)
Eye
Downward-slanting eyes
Flattened or missing cheekbones
Misshapen lower eyelids with missing eyelashes
Vision loss
Lower eyelid notch or cleft of missing lid tissue (lid coloboma)
Crossed eyes (strabismus)
Narrowed tear ducts (dacryostenosis)
Jaw
Cleft palate (opening in the roof of the mouth)
Underdeveloped lower jaw (Mandibular hypoplasia or micrognathia)
Misaligned teeth (Malocclusion)
Nose
Blocked or narrowed nasal passages (Choanal stenosis or atresia)
Large nose
Sleep Apnea (Respiratory insufficiency)
Narrowed throat passages (pharyngeal hypoplasia)
How is Treacher Collins Syndrome diagnosed?
The diagnosis of Treacher Collins syndrome is most often made by a pediatric expert following a thorough history and physical examination. Specific genetic testing or imaging is not required for the diagnosis. The craniofacial team at Children’s Health℠ will guide the type of tests your child may need based on their specific symptoms. These may include:
Airway imaging
Speech imaging
Audio testing for hearing deficiencies
Vision screening
Genetic testing
What are the causes of Treacher Collins Syndrome?
The exact cause of Treacher-Collins syndrome is unknown but it is understood to be the result of a genetic mutation. In the United States, approximately 1 in 50,000 people are affected with Treacher Collins syndrome.
How is Treacher Collins Syndrome treated?
When your child is diagnosed with Treacher Collins syndrome, they will be evaluated by an experienced craniofacial surgeon at Children’s Health to determine the best treatment plan. Our specialized team will take your child from infancy to adulthood, tailoring care to their unique needs. As issues arise, they will have access every year to:
Craniofacial surgeons
Orthodontics
Speech and feeding therapists
Oral-maxillary-facial surgeons
Ear-nose-throat specialist
Dentists
Social workers
Genetic experts
Psychologists
Efficient, coordinated treatment is done on one site and may include:
Surgery to reconstruct the facial bones
Air-way evaluations
Hearing assessments
Ear reconstruction
Speech therapy
Cleft palate repair
Bone grafting to palate
Orthodontics
Genetic evaluation
Treacher-Collins Syndrome Doctors and Providers
