"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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1999 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Syndactyly" by people in Profiles.
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Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
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Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. Hum Mol Genet. 1999 Aug; 8(8):1579-84.
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A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome. Genomics. 1991 Sep; 11(1):93-102.
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Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Genomics. 1989 May; 4(4):518-29.