What is Klippel-Feil Syndrome? Klippel-Feil Syndrome is a rare disorder characterized by the congenital fusion of two or more cervical (neck) vertebrae.
Klippel-Feil syndrome is a bone disorder characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae).
Important It is possible that the main title of the report Klippel - Feil Syndrome is not the name you expected. Please check the synonyms listing to find ...
The etiology of Klippel-Feil syndrome and its associated conditions is unknown. The syndrome can present with a variety of other clinical syndromes ...
Klippel-Feil Syndrome - Symptoms, Causes, Treatment, Life expectancy, Pictures and Photos. This syndrome is thought to occur very early in development of the fetus ...
Klippel–Feil syndrome is a rare disease, initially reported in 1912 by Maurice Klippel and André Feil from France,  characterized by the congenital fusion of ...
Klippel-Feil Syndrome (KFS) is a rare skeletal condition in which there is abnormal union or fusion (congenital synostosis) of two or more bones of the spinal column ...
Klippel-Feil syndrome (KFS) is a complex heterogeneous entity that results in cervical vertebral fusion. Two or more non-segmented cervical vertebrae are usually ...
General Discussion. Klippel-Feil syndrome (KFS) is a rare skeletal disorder primarily characterized by abnormal union or fusion of two or more bones of the spinal ...
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Klippel Feil syndrome