"Craniosynostoses" 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.
Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS.
| Descriptor ID |
D003398
|
| MeSH Number(s) |
C05.116.099.370.894.232 C05.660.207.240 C05.660.906.364 C16.131.621.207.240 C16.131.621.906.364
|
| Concept/Terms |
Craniosynostoses- Craniosynostoses
- Craniosynostose
- Craniosynostosis, Type 1
- 1 Craniosynostoses, Type
- 1 Craniosynostosis, Type
- Craniosynostoses, Type 1
- Type 1 Craniosynostoses
- Type 1 Craniosynostosis
- Plagiocephaly, Synostotic
- Synostotic Plagiocephaly
- Plagiocephaly, Craniosynostosis
- Craniosynostosis Plagiocephaly
- Craniosynostosis
- Craniostenosis
- Craniostenoses
Scaphocephaly- Scaphocephaly
- Sagittal Synostosis
- Sagittal Synostoses
- Synostoses, Sagittal
- Synostosis, Sagittal
Synostotic Anterior Plagiocephaly- Synostotic Anterior Plagiocephaly
- Anterior Plagiocephaly, Synostotic
- Plagiocephaly, Synostotic Anterior
- Unilateral Coronal Synostosis
- Coronal Synostoses, Unilateral
- Coronal Synostosis, Unilateral
- Synostoses, Unilateral Coronal
- Synostosis, Unilateral Coronal
- Unilateral Coronal Synostoses
Synostotic Posterior Plagiocephaly- Synostotic Posterior Plagiocephaly
- Plagiocephaly, Synostotic Posterior
- Posterior Plagiocephaly, Synostotic
- Craniosynostosis, Lambdoidal
- Craniosynostoses, Lambdoidal
- Lambdoidal Craniosynostoses
- Lambdoidal Craniosynostosis
- Lambdoid Synostosis
- Lambdoid Synostoses
- Synostoses, Lambdoid
- Synostosis, Lambdoid
Metopic Synostosis- Metopic Synostosis
- Metopic Synostoses
- Synostoses, Metopic
- Synostosis, Metopic
|
Below are MeSH descriptors whose meaning is more general than "Craniosynostoses".
Below are MeSH descriptors whose meaning is more specific than "Craniosynostoses".
This graph shows the total number of publications written about "Craniosynostoses" by people in this website by year, and whether "Craniosynostoses" 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 |
|---|
| 1993 | 1 | 0 | 1 |
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Craniosynostoses" by people in Profiles.
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González-Del Angel A, Estandía-Ortega B, Alcántara-Ortigoza MA, Martínez-Cruz V, Gutiérrez-Tinajero DJ, Rasmussen A, Gómez-González CS. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis. . 2016 12; 170(12):3189-3196.
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Deschamps-Braly J, Hettinger P, el Amm C, Denny AD. Volumetric analysis of cranial vault distraction for cephalocranial disproportion. Pediatr Neurosurg. 2011; 47(6):396-405.
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Panchal J, Amirsheybani H, Gurwitch R, Cook V, Francel P, Neas B, Levine N. Neurodevelopment in children with single-suture craniosynostosis and plagiocephaly without synostosis. Plast Reconstr Surg. 2001 Nov; 108(6):1492-8; discussion 1499-500.
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Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997 Mar; 60(3):555-64.
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Mooney MP, Aston CE, Siegel MI, Losken HW, Smith TD, Burrows AM, Wenger SL, Caruso K, Siegel B, Ferrell RE. Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits. J Craniofac Genet Dev Biol. 1996 Jan-Mar; 16(1):52-63.
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Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Further delineation of the Baller-Gerold syndrome. Am J Med Genet. 1993 Feb 15; 45(4):519-24.