Also known as: KFS, cervical vertebral fusion, Klippel-Feil anomaly
What is Klippel-Feil syndrome?
Klippel-Feil syndrome is a genetic disorder of the spine that is present at birth. In this condition, two or more vertebrae in the upper spinal column are fused together. This may or may not be symptomatic.
What causes Klippel-Feil syndrome?
The exact cause of Klippel-Feil syndrome isn’t clear. Some children seem to be more likely to get it based on their genetics. Some cases also appear to be hereditary and are passed down from parents to their children.
What are the symptoms of Klippel-Feil syndrome?
Sometimes children with klippel-Feil syndrome have stiffness in their neck. They may also have a short neck, trouble moving the neck and a low hairline at the back of the neck.
What are Klippel-Feil syndrome care options?
Treatment is patient specific, but usually consists of observation and avoiding certain activities. In severe cases, surgery may be needed.
Reviewed by: Stephen Graham George Jr., MD
This page was last updated on: 8/7/2018 9:37:25 AM
From the Newsdesk
Growing up, Haley Gantt suffered from scoliosis. She had to wear a back brace to prevent her curve from worsening, but unfortunately, she was later told that a spinal fusion surgery would have to be considered because the brace had failed to prevent the curve from progressing. She fought hard and got through it. An accomplished basketball player, Haley is now on her way to playing Division II basketball for Biola University in Southern California.
Learn about Scoliosis with Dr. Stephen George, Pediatric Orthopedic Surgeon, at Nicklaus Children's Hosptial.