"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 |
|---|
| 1998 | 0 | 1 | 1 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2013 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 2 | 3 |
| 2020 | 2 | 0 | 2 |
| 2021 | 2 | 0 | 2 |
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click here.
Below are the most recent publications written about "Acrocephalosyndactylia" by people in Profiles.
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Le Fort II Distraction with Simultaneous Zygomatic Repositioning. Clin Plast Surg. 2021 Jul; 48(3):487-496.
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Evolution of Cranioorbital Shape in Nonsyndromic, Muenke, and Saethre-Chotzen Bilateral Coronal Synostosis: A Case-Control Study of 2-Year Outcomes. Plast Reconstr Surg. 2021 01 01; 147(1):148-159.
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Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1. Am J Med Genet A. 2021 03; 185(3):916-922.
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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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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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Discussion: Airway Analysis in Apert Syndrome. Plast Reconstr Surg. 2019 09; 144(3):710-712.
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Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 03; 25(3):439-447.
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A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortality. Genet Med. 2019 02; 21(2):471-476.
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A Delayed Finding of a Tracheal Cartilaginous Sleeve in a Patient with Pfeiffer Syndrome Type 2 and a Complex Airway History. A A Case Rep. 2015 Aug 01; 5(3):36-9.
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Normalizing facial ratios in apert syndrome patients with Le Fort II midface distraction and simultaneous zygomatic repositioning. Plast Reconstr Surg. 2013 Jul; 132(1):129-140.