"Syndactyly" 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.
A congenital anomaly of the hand or foot, marked by the webbing between adjacent fingers or toes. Syndactylies are classified as complete or incomplete by the degree of joining. Syndactylies can also be simple or complex. Simple syndactyly indicates joining of only skin or soft tissue; complex syndactyly marks joining of bony elements.
Descriptor ID |
D013576
|
MeSH Number(s) |
C05.116.099.370.894.819 C05.660.585.800 C05.660.906.819 C16.131.621.585.800 C16.131.621.906.819
|
Concept/Terms |
Syndactyly- Syndactyly
- Syndactylies
- Syndactylia
- Syndactylias
|
Below are MeSH descriptors whose meaning is more general than "Syndactyly".
Below are MeSH descriptors whose meaning is more specific than "Syndactyly".
This graph shows the total number of publications written about "Syndactyly" by people in this website by year, and whether "Syndactyly" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2004 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2010 | 2 | 0 | 2 |
2011 | 0 | 1 | 1 |
2014 | 2 | 0 | 2 |
2015 | 2 | 0 | 2 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Syndactyly" by people in Profiles.
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TP63-related disorders: two case reports and a brief review of the literature. Dermatol Online J. 2021 Nov 15; 27(11).
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A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation. Am J Med Genet A. 2016 Mar; 170(3):728-33.
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Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes. Am J Med Genet A. 2015 Nov; 167A(11):2555-62.
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Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):622-32.
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Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation. J Invest Dermatol. 2014 Aug; 134(8):2146-2153.
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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. PLoS Genet. 2011 Jul; 7(7):e1002114.
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Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet. 2011 Jan 07; 88(1):70-5.
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A specific mutation in the distant sonic hedgehog (SHH) cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumb. Hum Mutat. 2010 Jan; 31(1):81-9.
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Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type? Am J Med Genet A. 2008 Sep 01; 146A(17):2308-11.
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The FU gene and its possible protein isoforms. BMC Genomics. 2004 Jul 22; 5(1):49.