"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 |
|---|
| 1995 | 1 | 0 | 1 |
| 1996 | 0 | 1 | 1 |
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Below are the most recent publications written about "Acrocephalosyndactylia" by people in Profiles.
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Distraction osteogenesis in maxillofacial surgery using internal devices: review of five cases. J Oral Maxillofac Surg. 1996 Jan; 54(1):45-53; discussion 54.
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Spatial dysmorphology of the foot in Apert syndrome: three-dimensional computed tomography. Cleft Palate Craniofac J. 1995 May; 32(3):255-61; discussion 262.
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Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. J Craniomaxillofac Surg. 1993 Jul; 21(5):181-8.
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Cerebral malformations in Carpenter syndrome. Pediatr Neurol. 1993 May-Jun; 9(3):230-4.
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Surgical correction of the craniofacial dysmorphology of Apert syndrome. Clin Plast Surg. 1991 Apr; 18(2):251-75.
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The craniofacial anatomy of Apert syndrome. Clin Plast Surg. 1991 Apr; 18(2):237-49.