"Klippel-Feil Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
Descriptor ID |
D007714
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MeSH Number(s) |
C05.116.099.370.535 C05.660.551 C16.131.621.551
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Concept/Terms |
Klippel-Feil Syndrome- Klippel-Feil Syndrome
- Klippel Feil Syndrome
- Syndrome, Klippel-Feil
- Vertebral Cervical Fusion Syndrome
- Klippel-Feil Sequence
- Dystrophia Brevicollis Congenita
- Dystrophia Brevicollis Congenitas
- Cervical Fusion Syndrome
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Below are MeSH descriptors whose meaning is more general than "Klippel-Feil Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Klippel-Feil Syndrome".
This graph shows the total number of publications written about "Klippel-Feil Syndrome" by people in this website by year, and whether "Klippel-Feil Syndrome" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Klippel-Feil Syndrome" by people in Profiles.
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Passias PG, Poorman GW, Jalai CM, Diebo BG, Vira S, Horn SR, Baker JF, Shenoy K, Hasan S, Buza J, Bronson W, Paul JC, Kaye I, Foster NA, Cassilly RT, Oren JH, Moskovich R, Line B, Oh C, Bess S, LaFage V, Errico TJ. Incidence of Congenital Spinal Abnormalities Among Pediatric Patients and Their Association With Scoliosis and Systemic Anomalies. J Pediatr Orthop. 2019 Sep; 39(8):e608-e613.