"Craniofacial Dysostosis" 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.
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.
Descriptor ID |
D003394
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MeSH Number(s) |
C05.116.099.370.231 C05.660.207.231 C16.131.621.207.231
|
Concept/Terms |
Craniofacial Dysostosis- Craniofacial Dysostosis
- Craniofacial Dysostosis Syndrome
- Craniofacial Dysostosis Syndromes
- Craniofacial Dysarthrosis
- Craniofacial Dysarthroses
- Dysarthroses, Craniofacial
- Dysarthrosis, Craniofacial
- Dysostosis, Craniofacial
- Craniofacial Dysostoses
- Dysostoses, Craniofacial
Crouzon Disease- Crouzon Disease
- Craniofacial Dysostosis, Type I
- Crouzon Craniofacial Dysostosis
- Craniofacial Dysostosis, Crouzon
- Craniofacial Dysostosis Type 1
- Crouzon's Disease
- Crouzons Disease
- Crouzon Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Craniofacial Dysostosis".
Below are MeSH descriptors whose meaning is more specific than "Craniofacial Dysostosis".
This graph shows the total number of publications written about "Craniofacial Dysostosis" by people in this website by year, and whether "Craniofacial Dysostosis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Craniofacial Dysostosis" by people in Profiles.
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Crouzon's Syndrome with a Dominant Sinus Pericranii Draining Transverse Sinus: Report of a Rare Association and Review of Literature. Pediatr Neurosurg. 2022; 57(3):196-201.
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Detection of important venous collaterals by computed tomography venogram in multisutural synostosis. Case report and review of the literature. J Neurosurg. 2007 Dec; 107(6 Suppl):508-10.
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A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Nat Genet. 1994 Jun; 7(2):149-53.