"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Acrocephalosyndactylia" by people in Profiles.
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Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects. Development. 2018 10 05; 145(19).
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A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome. Am J Med Genet A. 2017 10; 173(10):2838-2843.