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Bookmark or Share- Klippel–Feil syndrome - WikipediaKlippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck (cervical vertebrae).
- Klippel-Feil Syndrome (KFS) - Cleveland ClinicKlippel-Feil syndrome (KFS) is a condition in which you have two or more neck bones (vertebrae) fused together. KFS causes spine abnormalities and can affect many other body areas. Symptoms include short neck, limited neck mobility and low back-of-head hairline.
- Klippel-Feil syndrome | About the Disease | GARD - Genetic and Rare ...Klippel-Feil syndrome is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing. Genetic mutations may also result from contracted viruses, environmental factors, such as UV radiation from sunlight ...
- Klippel-Feil syndrome - Children's Hospital of PhiladelphiaKlippel-Feil syndrome is a rare bone disorder distinguished by the abnormal fusion of two or more bones in the neck. Children with the disorder may have a short, webbed neck, decreased range of motion in the head and neck area, and fusions in the thoracic spine causing scoliosis and/or kyphosis.
- Klippel Feil Syndrome - StatPearls - NCBI BookshelfKlippel-Feil syndrome is a complex, congenital condition characterized by the abnormal fusion of 2 or more cervical vertebrae due to the failure of proper segmentation during early fetal development.
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