 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 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
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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 |
|---|
| 2005 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2016 | 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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Walklate J, Vera C, Bloemink MJ, Geeves MA, Leinwand L. The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects. J Biol Chem. 2016 May 06; 291(19):10318-31.
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Chong JX, McMillin MJ, Shively KM, Beck AE, Marvin CT, Armenteros JR, Buckingham KJ, Nkinsi NT, Boyle EA, Berry MN, Bocian M, Foulds N, Uzielli ML, Haldeman-Englert C, Hennekam RC, Kaplan P, Kline AD, Mercer CL, Nowaczyk MJ, Klein Wassink-Ruiter JS, McPherson EW, Moreno RA, Scheuerle AE, Shashi V, Stevens CA, Carey JC, Monteil A, Lory P, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ. De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay. Am J Hum Genet. 2015 Mar 05; 96(3):462-73.
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Herrmann BW, Karzon R, Molter DW. Otologic and audiologic features of Nager acrofacial dysostosis. Int J Pediatr Otorhinolaryngol. 2005 Aug; 69(8):1053-9.
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Gollin YG, Abuhamad AZ, Inati MN, Shaffer WK, Copel JA, Hobbins JC. Sonographic appearance of craniofacial dysostosis (Crouzon syndrome) in the second trimester. J Ultrasound Med. 1993 Oct; 12(10):625-8.
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Chervenak FA, Tortora M, Mayden K, Mesologites T, Isaacson G, Mahoney MJ, Hobbins JC. Antenatal diagnosis of median cleft face syndrome: sonographic demonstration of cleft lip and hypertelorism. Am J Obstet Gynecol. 1984 May 01; 149(1):94-7.
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Mayden KL, Tortora M, Berkowitz RL, Bracken M, Hobbins JC. Orbital diameters: a new parameter for prenatal diagnosis and dating. Am J Obstet Gynecol. 1982 Oct 01; 144(3):289-97.
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