"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
|
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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1995 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Craniofacial Dysostosis" by people in Profiles.
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An unusual presentation of bilateral optic pathway glioma in Crouzon Syndrome. Pediatr Hematol Oncol. 2023; 40(8):800-806.
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Craniosynostotic variations in syndromic, identical twins. Ann Plast Surg. 2008 Sep; 61(3):290-3.
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Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome. Eur J Hum Genet. 2005 May; 13(5):528-40.
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Surgical management of V-pattern strabismus and oblique dysfunction in craniofacial dysostosis. J AAPOS. 2000 Dec; 4(6):338-42.
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Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis. Nat Genet. 1995 Sep; 11(1):40-4.
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Extensive wormian bones in a patient with the Hallermann-Streiff syndrome. J Child Neurol. 1990 Jan; 5(1):50-1.
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Congenital ophthalmoplegia in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome). A clinicopathologic study and review of the literature. Neurology. 1976 Jul; 26(7):638-44.
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Unilateral arhinencephaly in goldenhar-gorlin syndrome. Dev Med Child Neurol. 1975 Aug; 17(4):498-504.