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Klippel Feil Syndrome |
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Klippel Feil Syndrome (KFS) is a rare disorder characterized by the congenital fusion of any 2 of the 7 cervical vertebrae. It is caused by a failure in the normal segmentation of the cervical vertebrae during the early weeks of fetal development. The most common signs of the disorder are short neck, low hairline at the back of the head, and restricted mobility of the upper spine.
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Klippel Feil Syndrome Other1 of 1
Klippel Feil Syndrome Information Page
... Klippel-Feil Syndrome is a rare disorder characterized by the congenital fusion of any 2 of the 7 cervical (neck) vertebrae. It is caused by a failure in the normal segmentation or division of the cer...
Source: National Institute of Neurological Disorders and Stroke
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Klippel Feil Syndrome Articles
- Klippel Feil Syndrome Information Page
... Klippel-Feil Syndrome is a rare disorder characterized by the congenital fusion of any 2 of the 7 cervical (neck) vertebrae. It is caused by a failure in the normal segmentation or division of the cer...
Resources
- Klippel Feil Syndrome (National Institute of Neurological Disorders and Stroke)
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