 Craniofacial Dysostosis
"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
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| Concept/Terms |
Craniofacial Dysostosis- Craniofacial Dysostosis
- Craniofacial Dysostoses
- Dysostoses, Craniofacial
- Dysostosis, Craniofacial
Crouzon Disease- Crouzon Disease
- Crouzon's Disease
- Crouzon Syndrome
- Craniofacial Dysostosis Type 1
- Crouzon Craniofacial Dysostosis
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1983 | 0 | 1 | 1 | | 1984 | 1 | 0 | 1 | | 1985 | 0 | 1 | 1 | | 1987 | 1 | 0 | 1 | | 1991 | 1 | 0 | 1 | | 1993 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1999 | 1 | 0 | 1 | | 2000 | 0 | 1 | 1 | | 2011 | 1 | 0 | 1 | | 2018 | 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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Matuszewska KE, Badura-Stronka M, Smigiel R, Cabala M, Biernacka A, Kosinska J, Rydzanicz M, Winczewska-Wiktor A, Sasiadek M, Latos-Bielenska A, Zemojtel T, Ploski R. Phenotype of two Polish patients with Schaaf-Yang syndrome confirmed by identifying mutation in MAGEL2 gene. Clin Dysmorphol. 2018 Apr; 27(2):49-52.
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Ionita-Laza I, Makarov V, Yoon S, Raby B, Buxbaum J, Nicolae DL, Lin X. Finding disease variants in Mendelian disorders by using sequence data: methods and applications. Am J Hum Genet. 2011 Dec 09; 89(6):701-12.
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Vannier MW. Evaluation of 3D imaging. Crit Rev Diagn Imaging. 2000 Oct; 41(5):315-78.
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Waggoner DJ, Ciske DJ, Dowton SB, Watson MS. Deletion of 1q in a patient with acrofacial dysostosis. Am J Med Genet. 1999 Feb 12; 82(4):301-4.
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Lo LJ, Marsh JL, Yoon J, Vannier MW. Stability of fronto-orbital advancement in nonsyndromic bilateral coronal synostosis: a quantitative three-dimensional computed tomographic study. Plast Reconstr Surg. 1996 Sep; 98(3):393-405; discussion 406-9.
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Kreiborg S, Marsh JL, Cohen MM, Liversage M, Pedersen H, Skovby F, Børgesen SE, Vannier MW. Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. J Craniomaxillofac Surg. 1993 Jul; 21(5):181-8.
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Stevenson GW, Hall SC, Bauer BS, Vicari FA, Seleny FL. Anaesthetic management of Miller's syndrome. Can J Anaesth. 1991 Nov; 38(8):1046-9.
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Marsh JL, Vannier MW. The anatomy of the cranio-orbital deformities of craniosynostosis: insights from 3-D images of CT scans. Clin Plast Surg. 1987 Jan; 14(1):49-60.
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Corey JP, Caldarelli DD, Gould HJ. Otopathology in cranial facial dysostosis. Am J Otol. 1987 Jan; 8(1):14-7.
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Marsh JL, Vannier MW, Stevens WG, Warren JO, Gayou D, Dye DM. Computerized imaging for soft tissue and osseous reconstruction in the head and neck. Clin Plast Surg. 1985 Apr; 12(2):279-91.
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