 Syndactyly
"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
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| 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
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| Concept/Terms |
Syndactyly- Syndactyly
- Syndactylies
- Syndactylia
- Syndactylias
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 1 | 2 | | 2006 | 0 | 1 | 1 | | 2012 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 | | 2016 | 0 | 1 | 1 | | 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Syndactyly" by people in Profiles.
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Sanderson JL, Freund RK, Castano AM, Benke TA, Dell'Acqua ML. The CaV1.2 G406R mutation decreases synaptic inhibition and alters L-type Ca2+ channel-dependent LTP at hippocampal synapses in a mouse model of Timothy Syndrome. Neuropharmacology. 2022 Dec 01; 220:109271.
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Karasik D, Rivadeneira F, Johnson ML. The genetics of bone mass and susceptibility to bone diseases. Nat Rev Rheumatol. 2016 Jun; 12(6):323-34.
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Saari J, Lovell MA, Yu HC, Bellus GA. Compound heterozygosity for a frame shift mutation and a likely pathogenic sequence variant in the planar cell polarity?ciliogenesis gene WDPCP in a girl with polysyndactyly, coarctation of the aorta, and tongue hamartomas. Am J Med Genet A. 2015 Feb; 167A(2):421-7.
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Schnatwinkel C, Niswander L. Nubp1 is required for lung branching morphogenesis and distal progenitor cell survival in mice. PLoS One. 2012; 7(9):e44871.
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Geurts AM, Collier LS, Geurts JL, Oseth LL, Bell ML, Mu D, Lucito R, Godbout SA, Green LE, Lowe SW, Hirsch BA, Leinwand LA, Largaespada DA. Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers. PLoS Genet. 2006 Sep 29; 2(9):e156.
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Oates SD, Gosain AK. Syndactyly repair performed simultaneously with circumcision: use of foreskin as a skin-graft donor site. J Pediatr Surg. 1997 Oct; 32(10):1482-4.
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De Smet L, Matton G, Monstrey S, Cambier E, Fabry G. Application of the IFSSH(3)-classification for congenital anomalies of the hand; results and problems. Acta Orthop Belg. 1997 Sep; 63(3):182-8.
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