|
|
|
CraniosynostosisCraniosynostosis means fused bones of the skull. It is a condition that some children are born with and some develop later. A child's skull grows very rapidly during the first two years of life. Different bones that fit together like a jigsaw puzzle make up the skull. The areas where the bones meet one another are called sutures. When one of these sutures is fused too early, it is called craniosynostosis. When this happens, further growth in this area cannot occur. This may lead to overgrowth in another area, which results in an abnormally shaped skull. Surgery to correct craniosynostosis is best performed within the first three to six months of life. |
|
Crouzon's Syndrome This is a condition in which sutures in the head are prematurely fused resulting in abnormal growth of the skull and face. The growth of the middle portion of the child's face does not keep up with the jaw, resulting in very irregular facial characteristics, such as bulging eyes, an upper jaw that is too far back and a lower jaw that is too far forward. They may have problems with teeth due to abnormal jaw growth.This can be corrected surgically by advancing the middle portion of the face, thus increasing the ability to cover the teeth and protect the eyes while giving a more pleasing appearance. |
|
Apert's Syndrome Apert's syndrome also results from premature fusion of the skull that causes abnormal growth of the skull and face. Syndactyly which is the fusion of the fingers and commonly known as webbing, is found with this syndrome. Children with Apert's have bulging eyes that are usually wide-set and tilted down at the sides. They usually have problems with teeth alignment due to the underdevelopment of the upper jaw. Surgery can also be performed to separate the fingers. This should be done as early as possible to increase the fingers' functional potential. |
|
Treacher-Collins' Syndrome This syndrome is characterized by lack of bone development in the cheeks and around the eyes, causing the eyes and eyelids to droop at the sides. This syndrome also creates complex problems with the jaw and upper dental arch that require complex corrective surgery. Significant improvement can be obtained with craniofacial surgery. |
|
Orbital HypertelorismThis is a condition in which the position of the bones around the eyes is further to the side than the normal position, causing the eyes to be too far apart and grossly deforming the appearance. This can be corrected with a procedure called an orbital osteotomy. The excess bone between the eyes is removed, and the bone containing the eyes is moved back toward the middle of the face. |
|
|
|
|
|
|
|
|
|
2200 Children's Way | Nashville, Tenn. 37232 | 615.936.1000
© 2013 Monroe Carell Jr. Children's Hospital at Vanderbilt




Cleft Lip and Palate
Craniosynostosis
Crouzon's Syndrome
Apert's Syndrome
Treacher-Collins' Syndrome
Orbital Hypertelorism
Dental Deformities
Temporomandibular Joint Disorders (TMJ)
Head and Neck Oncology