 Limb Deformities, Congenital
"Limb Deformities, Congenital" 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.
Congenital structural deformities of the upper and lower extremities collectively or unspecified.
| Descriptor ID |
D017880
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| MeSH Number(s) |
C05.660.585 C16.131.621.585
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| Concept/Terms |
Limb Deformities, Congenital- Limb Deformities, Congenital
- Congenital Limb Deformities
- Congenital Limb Deformity
- Deformities, Congenital Limb
- Deformity, Congenital Limb
- Limb Deformity, Congenital
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Below are MeSH descriptors whose meaning is more general than "Limb Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Limb Deformities, Congenital".
This graph shows the total number of publications written about "Limb Deformities, Congenital" by people in this website by year, and whether "Limb Deformities, Congenital" 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 |
|---|
| 1999 | 0 | 1 | 1 | | 2003 | 1 | 0 | 1 | | 2005 | 1 | 1 | 2 | | 2013 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Limb Deformities, Congenital" by people in Profiles.
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Truong BT, Shull LC, Lencer E, Bend EG, Field M, Blue EE, Bamshad MJ, Skinner C, Everman D, Schwartz CE, Flanagan-Steet H, Artinger KB. PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation. Dis Model Mech. 2023 04 01; 16(4).
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Truong BT, Artinger KB. The power of zebrafish models for understanding the co-occurrence of craniofacial and limb disorders. Genesis. 2021 02; 59(1-2):e23407.
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Shi H, Enriquez A, Rapadas M, Martin EMMA, Wang R, Moreau J, Lim CK, Szot JO, Ip E, Hughes JN, Sugimoto K, Humphreys DT, McInerney-Leo AM, Leo PJ, Maghzal GJ, Halliday J, Smith J, Colley A, Mark PR, Collins F, Sillence DO, Winlaw DS, Ho JWK, Guillemin GJ, Brown MA, Kikuchi K, Thomas PQ, Stocker R, Giannoulatou E, Chapman G, Duncan EL, Sparrow DB, Dunwoodie SL. NAD Deficiency, Congenital Malformations, and Niacin Supplementation. N Engl J Med. 2017 08 10; 377(6):544-552.
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Gupta A, Bischoff A. Pathology of cloaca anomalies with case correlation. Semin Pediatr Surg. 2016 Apr; 25(2):66-70.
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Han YC, Vidigal JA, Mu P, Yao E, Singh I, Gonz?lez AJ, Concepcion CP, Bonetti C, Ogrodowski P, Carver B, Selleri L, Betel D, Leslie C, Ventura A. An allelic series of miR-17 ~ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron. Nat Genet. 2015 Jul; 47(7):766-75.
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Kochhar A, Kirmani S, Cetta F, Younge B, Hyland JC, Michels V. Similarity of geleophysic dysplasia and Weill-Marchesani syndrome. Am J Med Genet A. 2013 Dec; 161A(12):3130-2.
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Wilson WD, Johnson PT, Sutherland DR, Mon? H, Loker ES. A molecular phylogenetic study of the genus Ribeiroia (Digenea): trematodes known to cause limb malformations in amphibians. J Parasitol. 2005 Oct; 91(5):1040-5.
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Herrmann BW, Karzon R, Molter DW. Otologic and audiologic features of Nager acrofacial dysostosis. Int J Pediatr Otorhinolaryngol. 2005 Aug; 69(8):1053-9.
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Johnson PT, Sutherland DR. Amphibian deformities and Ribeiroia infection: an emerging helminthiasis. Trends Parasitol. 2003 Aug; 19(8):332-5.
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Mills AA, Zheng B, Wang XJ, Vogel H, Roop DR, Bradley A. p63 is a p53 homologue required for limb and epidermal morphogenesis. Nature. 1999 Apr 22; 398(6729):708-13.
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