Klippel-feil Syndrome

Klippel-Feil syndrome is a rare bone disorder. During early fetal development, the normal division of the cervical vertebrae (spinal bones in the neck) fails, resulting in Klippel-Fiel syndrome. As a result, two or more cervical vertebrae are abnormally fused from birth. Short neck, restricted upper spine movement, and low hairline (at the back) are commonly seen in such patients. Some patients may experience nerve damage and pain due to the fused vertebrae. Treatment is symptomatic and includes surgery and physical therapy.

  
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My kid has Klippel-Feil syndrome. How to relieve spine issues?

Query: Hi doctor, My nine-month-old infant has Klippel-Feil syndrome. She has multilevel issues throughout her spine and would like you to review the submitted information and let us know your thoughts. We believe she also has a hemivertebra that is fully segmented at the right C5.  Read Full »


Answer: Hello, Welcome to icliniq.com. I understand your concern. I reviewed the image and reports you uploaded (attachment removed to protect the patient's identity). The most concerning here is a deformity in the spine. There is a defect in the formation of multiple vertebrae, which is responsible for t...  Read Full »

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