Klippel-Feil Syndrome

A syndrome characterised by a low hairline and a shortened neck resulting from a reduced number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass.

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Subheadings:

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C05.116.099.370.535, C05.660.551, C16.131.621.551

MeSH Unique ID: D007714

Entry Terms:

• Klippel Feil Syndrome
• Syndrome, Klippel-Feil
• Dystrophia Brevicollis Congenita
• Dystrophia Brevicollis Congenitas
• Cervical Fusion Syndrome
• Klippel-Feil Sequence
• Vertebral Cervical Fusion Syndrome

All MeSH Categories
Diseases Category
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Klippel-Feil Syndrome

All MeSH Categories
Diseases Category
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Klippel-Feil Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Klippel-Feil Syndrome