"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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2021 | 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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Genetics of craniofacial malformations. Semin Fetal Neonatal Med. 2021 12; 26(6):101290.
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De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Am J Hum Genet. 2017 Nov 02; 101(5):833-843.
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A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes. Sci Rep. 2017 03 10; 7:44138.
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Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum. Am J Med Genet A. 2016 May; 170A(5):1295-301.
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De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. Nat Genet. 2011 Jun 26; 43(8):729-31.
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Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis. Eur J Hum Genet. 2011 May; 19(5):513-9.
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Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet. 2011 Jan 07; 88(1):70-5.
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Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type? Am J Med Genet A. 2008 Sep 01; 146A(17):2308-11.
MeSH information
