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Concept information

disease > congenital disease > malformation > Klippel-Feil syndrome
disease > genetic disease > hereditary disease > Klippel-Feil syndrome
disease > congenital disease > malformation > dysostosis > Klippel-Feil syndrome
disease > diseases of the osteoarticular system > dysostosis > Klippel-Feil syndrome
disease > diseases of the osteoarticular system > spine disease > Klippel-Feil syndrome

Terme préférentiel

Klippel-Feil syndrome  

Définition

  • Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare condition present at birth (congenital disease) characterized by the abnormal joining (fusion) of any two of the seven bones in the neck (cervical vertebrae). (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-D4VR1G17-D

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