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Connect with the Norton Children’sNeurosurgery Team
(502) 583-1697
The board-certified neurosurgical team with Norton Children’s Neuroscience Institute, affiliated with the UofL School of Medicine, is led by Thomas M. Moriarty, M.D., Ph.D., a recognized leader in the field with extensive experience and specialized training. Our physicians in Louisville and Southern Indiana have the sophisticated tools and skills to give you and your child a precise diagnosis and treatment plan for craniosynostosis that minimizes risk, so your child can get back to being a kid again.
A newborn’s skull consists of several plates of bone that fuse together over time. When two or more of these plates fuse together before they are supposed to, they can cause the baby’s head to become misshapen. It’s not clear why craniosynostosis happens. It may be an inherited trait in some families. However, studies have not concluded why it occurs.
In some cases, craniosynostosis can lead to developmental delays and cognitive issues, but you should not assume the worst. It all depends on a variety of factors, including when the condition was diagnosed, how many plates are involved and whether any intracranial pressure occurred. The specialists at Norton Children’s Hospital are experienced in treating craniosynostosis in infants and children. They are the best people to talk to about potential long-term effects.
Types of craniosynostosis are named for which skull plates are affected. Each type results in a different misshapen look to the head. Sagittal craniosynostosis is the most common of four types. It results in the head growing long and narrow, because it’s caused by the fusion of the line (suture) that runs along the top of the baby’s skull. This can cause the baby’s skull to appear boat-shaped.
Metopic synostosis is the fusion of the metopic suture, which runs from the top of the head down the middle of the forehead, toward the nose. The condition causes:
Coronal synostosis is the premature fusion of one of the coronal sutures, which extend from ear to ear over the top of the head. Characteristics include:
Bicoronal synostosis results when both coronal sutures fuse prematurely. Characteristics include:
Regardless of the type, craniosynostosis can be treated.
Unless it is a mild case, craniosynostosis is corrected with surgery. The multidisciplinary team of physicians in our craniofacial program, including neurosurgeons, plastic surgeons and ear, nose and throat physicians, work together to plan the best procedure to treat your child’s craniosynostosis. If detected early, the fused sutures can sometimes be released using limited or smaller incisions, called an endoscope.
If craniosynostosis is diagnosed later or is more advanced, it can be repaired with an open procedure in which the bone is expanded with absorbable plates. In some cases, the craniofacial team will elect to release the suture and place bone-expanding devices that penetrate through the skin until the expansion is complete.
Regular monitoring may be required. The experienced pediatric surgeons and physicians with the craniofacial program will be there every step of the way.
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