"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
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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
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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
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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 |
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2006 | 2 | 0 | 2 |
2007 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2019 | 0 | 2 | 2 |
2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Acrocephalosyndactylia" by people in Profiles.
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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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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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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 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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Variable expressivity and clinical heterogeneity can complicate the diagnosis and management of Pfeiffer syndrome. J Craniofac Surg. 2013; 24(5):1829-32.
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Apert syndrome with fused thalami. Fetal Pediatr Pathol. 2012 Dec; 31(6):410-4.
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Normal and disease-related biological functions of Twist1 and underlying molecular mechanisms. Cell Res. 2012 Jan; 22(1):90-106.
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Tracheal anomalies complicating ventilation of an infant with Apert syndrome. J Clin Anesth. 2007 Nov; 19(7):551-4.
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Congenital nasal malformations. Otolaryngol Clin North Am. 2007 Feb; 40(1):97-112, vi-vii.
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Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. J AAPOS. 2006 Dec; 10(6):521-7.