"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 1 | 2 |
| 2010 | 1 | 0 | 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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Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblings. Exp Mol Pathol. 2020 08; 115:104471.
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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud. Genet Med. 2020 01; 22(1):189-198.
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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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An atypical case of Klippel-Tr?naunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report. BMC Pediatr. 2019 04 06; 19(1):95.
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Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. Mol Genet Genomic Med. 2019 02; 7(2):e00501.
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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.