"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
|
| MeSH Number(s) |
C05.116.099.370.535 C05.660.551 C16.131.621.551
|
| 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
|
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 |
|---|
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Klippel-Feil Syndrome" by people in Profiles.
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Giampietro PF, Armstrong L, Stoddard A, Blank RD, Livingston J, Raggio CL, Rasmussen K, Pickart M, Lorier R, Turner A, Sund S, Sobrera N, Neptune E, Sweetser D, Santiago-Cornier A, Broeckel U. Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes. Am J Med Genet A. 2015 Jan; 167A(1):95-102.