"Polydactyly" 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 presence of supernumerary digits.
| Descriptor ID |
D017689
|
| MeSH Number(s) |
C05.660.585.600 C16.131.621.585.600
|
| Concept/Terms |
Polydactyly- Polydactyly
- Polydactylies
- Polydactylia
- Polydactylias
- Polydactylism
- Polydactylisms
- Hyperdactyly
- Hyperdactylies
|
Below are MeSH descriptors whose meaning is more general than "Polydactyly".
Below are MeSH descriptors whose meaning is more specific than "Polydactyly".
This graph shows the total number of publications written about "Polydactyly" by people in this website by year, and whether "Polydactyly" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 3 | 0 | 3 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polydactyly" by people in Profiles.
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De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. Am J Med Genet A. 2022 08; 188(8):2360-2366.
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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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Severe presentation and complex brain malformations in an individual carrying a CCND2 variant. Mol Genet Genomic Med. 2019 06; 7(6):e708.
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Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly. Hum Genet. 2019 Jun; 138(6):593-600.
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FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. J Bone Miner Res. 2019 02; 34(2):375-386.
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"On-Top Plasty" for Radial Polydactyly?Reconstruction. J Hand Surg Am. 2017 Sep; 42(9):753.e1-753.e6.
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Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI. Orphanet J Rare Dis. 2012 Jan 11; 7:4.
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Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies. Pediatr Res. 2008 Jan; 63(1):9-14.
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Re: clinical report by Ahmad et al. 14q(22) deletion in a familial case of anophthalmia with polydactyly. Am J Med Genet A. 2004 Apr 01; 126A(1):109; author reply 110.
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Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice. Mamm Genome. 2001 Oct; 12(10):796-8.