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.
MeSH Number(s)
C05.660.585
C16.131.621.585
Concept/Terms
Limb Deformities, Congenital- Limb Deformities, Congenital
- Congenital Limb Deformities
- Congenital Limb Deformity
- Deformities, Congenital Limb
- Deformity, Congenital Limb
- Limb Deformity, Congenital
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 Harvard Catalyst Profiles by year, and whether "Limb Deformities, Congenital" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 1996 | 0 | 1 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 4 | 3 | 7 |
| 2000 | 2 | 0 | 2 |
| 2001 | 1 | 2 | 3 |
| 2002 | 2 | 1 | 3 |
| 2003 | 2 | 1 | 3 |
| 2004 | 1 | 0 | 1 |
| 2005 | 2 | 0 | 2 |
| 2006 | 0 | 3 | 3 |
| 2007 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 1 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 4 | 1 | 5 |
| 2012 | 6 | 2 | 8 |
| 2013 | 6 | 1 | 7 |
| 2014 | 2 | 1 | 3 |
| 2015 | 2 | 0 | 2 |
| 2016 | 4 | 3 | 7 |
| 2017 | 1 | 0 | 1 |
| 2018 | 3 | 2 | 5 |
| 2019 | 2 | 0 | 2 |
| 2020 | 2 | 0 | 2 |
| 2021 | 4 | 1 | 5 |
| 2022 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
Below are the most recent publications written about "Limb Deformities, Congenital" by people in Profiles.
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Sequence variants in DLX5, HOXD13 and 445?kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families. Clin Genet. 2024 Jan; 105(1):109-111.
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Does presence of a VACTERL anomaly predict an associated gynecologic anomaly in females with anorectal malformations?: A Pediatric Colorectal and Pelvic Learning Consortium Study. J Pediatr Surg. 2023 Mar; 58(3):471-477.
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Hypothesis: Central digit hypoplasia. Am J Med Genet A. 2022 06; 188(6):1746-1751.
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Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms. Clin Genet. 2021 11; 100(5):615-623.
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Terminal transverse limb defects. Birth Defects Res. 2021 08 01; 113(13):1029-1030.
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Terminal transverse limb defects with "nubbins". Birth Defects Res. 2021 08 01; 113(13):1007-1014.
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Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth. Genet Med. 2021 10; 23(10):1882-1888.
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UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly. Genet Med. 2021 09; 23(9):1624-1635.
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Digital Transfer for Hand Reconstruction in Cleft Hand and Foot Differences. J Reconstr Microsurg. 2021 Sep; 37(7):589-596.
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Depiction of ectrodactyly, sirenomelia and cyclopia in a figure by Hokusai. Am J Med Genet C Semin Med Genet. 2021 06; 187(2):148-150.