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Treacher-Collins syndrome Health Article
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Definition
Treacher-Collins syndrome is a hereditary condition that causes facial defects.
Alternative Names
Causes, incidence, and risk factors
Treacher-Collins syndrome is caused by a defective protein called treacle. The condition is inherited as an autosomal dominant trait. More than half of all cases are thought to be due to new mutations because there is no family history of the disease. This condition may greatly vary in severity from generation to generation.
Symptoms
Signs and tests
The child usually will show normal intelligence. Examination of the infant may reveal a variety of problems, including: Genetic tests can be done to look for mutations on the TCS1 gene.
Treatment
Treatment consists of testing for and treating any hearing loss so that a child can perform up to normal level in school. Plastic surgery can address the receding chin and other defects.
Support Groups
Treacher Collins Foundation -- www.treachercollinsfnd.org
Expectations (prognosis)
Children with this syndrome typically grow to become normally functioning adults of normal intelligence. Careful attention to any hearing problems helps ensure better performance in school.
Complications
Calling your health care provider
This condition is usually apparent at birth. Call your health care provider if you have a child with Treacher-Collins syndrome and the hearing appears to be worse, or if other problems arise. A good plastic surgeon is very important, as there is sometimes a need for a series of operations over years to correct birth defects.
Prevention
Genetic counseling is appropriate for prospective parents with a family history of Treacher-Collins syndrome. |
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