"Acrocephalosyndactylia" 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.
Congenital craniostenosis with syndactyly.
| Descriptor ID |
D000168
|
| MeSH Number(s) |
C05.116.099.370.894.232.015 C05.116.099.370.894.819.100 C05.660.207.240.100 C05.660.585.800.100 C05.660.906.364.100 C05.660.906.819.100 C16.131.621.207.240.100 C16.131.621.585.800.100 C16.131.621.906.364.100 C16.131.621.906.819.100
|
| Concept/Terms |
Acrocephalosyndactylia- Acrocephalosyndactylia
- Acrocephalosyndactylias
- Kurczynski Casperson Syndrome
- Syndrome, Kurczynski Casperson
Apert-Crouzon Disease- Apert-Crouzon Disease
- Apert Crouzon Disease
- Disease, Apert-Crouzon
- Acrocephalosyndactyly, Type II
- Acrocephalosyndactylies, Type II
- Type II Acrocephalosyndactylies
- Type II Acrocephalosyndactyly
Saethre-Chotzen Syndrome- Saethre-Chotzen Syndrome
- Saethre Chotzen Syndrome
- Syndrome, Saethre-Chotzen
- Acrocephaly, Skull Asymmetry, and Mild Syndactyly
- Acrocephalosyndactyly III
- Acrocephalosyndactyly IIIs
- Acrocephalosyndactyly, Type III
- Acrocephalosyndactylies, Type III
- Type III Acrocephalosyndactyly
- Dysostosis Craniofacialis with Hypertelorism
- Acrocephalosyndactyly, Type 3
- Acrocephalosyndactylies, Type 3
- Chotzen Syndrome
- Syndrome, Chotzen
Apert Syndrome- Apert Syndrome
- Syndrome, Apert
- Acrocephalosyndactyly (Apert)
- Acrocephalosyndactyly, Type I
- Acrocephalosyndactylies, Type I
- Type I Acrocephalosyndactylies
- Type I Acrocephalosyndactyly
- Acrocephalosyndactyly, Type 1
- Acrocephalosyndactylies, Type 1
- Syndactylic Oxycephaly
- Syndactylic Oxycephalies
Pfeiffer Syndrome- Pfeiffer Syndrome
- Syndrome, Pfeiffer
- Noack Syndrome
- Noack Syndromes
- Syndrome, Noack
- Syndromes, Noack
- Craniofacial-Skeletal-Dermatologic Dysplasia
- Acrocephalosyndactyly, Type V
- Acrocephalosyndactylies, Type V
- Type V Acrocephalosyndactylies
- Type V Acrocephalosyndactyly
|
Below are MeSH descriptors whose meaning is more general than "Acrocephalosyndactylia".
Below are MeSH descriptors whose meaning is more specific than "Acrocephalosyndactylia".
This graph shows the total number of publications written about "Acrocephalosyndactylia" by people in this website by year, and whether "Acrocephalosyndactylia" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 3 | 0 | 3 |
| 1997 | 3 | 0 | 3 |
| 1998 | 2 | 0 | 2 |
| 1999 | 2 | 0 | 2 |
| 2000 | 2 | 0 | 2 |
| 2001 | 1 | 1 | 2 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 1 | 2 |
| 2006 | 3 | 1 | 4 |
| 2007 | 2 | 2 | 4 |
| 2008 | 1 | 0 | 1 |
| 2009 | 5 | 0 | 5 |
| 2010 | 4 | 0 | 4 |
| 2012 | 1 | 1 | 2 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2016 | 2 | 0 | 2 |
| 2018 | 2 | 0 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
| 2024 | 3 | 0 | 3 |
Below are the most recent publications written about "Acrocephalosyndactylia" by people in Profiles.
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Long-term photogrammetric outcomes of midface advancement in Apert syndrome: are we nearing normal? Childs Nerv Syst. 2024 Dec; 40(12):4023-4032.
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The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. Eur J Hum Genet. 2024 Jul; 32(7):864-870.
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The influence of orbital architecture on strabismus in craniosynostosis. J AAPOS. 2024 02; 28(1):103812.
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The developing mouse coronal suture at single-cell resolution. Nat Commun. 2021 08 10; 12(1):4797.
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Timing of Ossification of the Anterior Skull Base in Syndromic Synostosis. J Craniofac Surg. 2020 Jul-Aug; 31(5):1256-1260.
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Craniofacial abnormalities in a murine model of Saethre-Chotzen Syndrome. Ann Anat. 2019 Sep; 225:33-41.
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Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome. Elife. 2018 10 25; 7.
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Tyrosine kinase receptor c-ros-oncogene 1 inhibition alleviates aberrant bone formation of TWIST-1 haploinsufficient calvarial cells from Saethre-Chotzen syndrome patients. J Cell Physiol. 2018 09; 233(9):7320-7332.
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The ophthalmic sequelae of Pfeiffer syndrome and the long-term visual outcomes after craniofacial surgery. J AAPOS. 2016 08; 20(4):315-9.
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Apert Syndrome: Outcomes From the Australian Craniofacial Unit's Birth to Maturity Management Protocol. J Craniofac Surg. 2016 Jul; 27(5):1125-34.