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Klippel-Feil Syndrome

Known as: feil klippel syndrome, Klippel-Feil Sequence, TORTICOLLIS, OSSEOUS CONGENITAL 
A rare congenital syndrome characterized by the fusion of the vertebrae in the cervical spine. Patients present with a short neck and restricted… 
National Institutes of Health

Papers overview

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1996
1996
Klippel-Feil syndrome (KFS) is characterised by congenital fusion of vertebrae within the rostral spine. The first KFS gene (SGM1… 
Review
1994
Review
1994
We report a case of a 45-year-old man with Klippel-Feil syndrome with fusion of the C2–3 and C4–5 cervical vertebrae and severe… 
1983
1983
A young girl with Klippel-Feil syndrome presented with the onset of mirror movements in early childhood. Computerized tomography… 
1972
1972
Klippel-Feil syndrome, the triad of limitation of movement of the head, short neck, and low posterior hairline, is often… 
1971
1971
Two cases of Klippel-Feil syndrome are reported, both of which have congenital absence of one kidney and various other anomalies… 
Review
1961
Review
1961
In 1912, Klippel and Feil described the pathologic anatomy of the absence of the neck in a 46-year-old man.1Including cases… 
1958
1958
D.H. is the second child of healthy parents, the elder child being normal. He was first referred to the Children's Hospital in… 
Review
1936
Review
1936
Hitherto, reports of cases of the Klippel-Feil syndrome have considered only the clinical manifestations. These have been… 
1934
1934
Congenital anomalies of the vertebrae are not very uncommon, especially in the lumbar region. Those of the cervical region are… 
Highly Cited
1932
Highly Cited
1932
Anomalies in the cervical spine are uncommon; especially rare are those described under the obscure term of the Klippel-Feil…